National Medical Care, Medical Products Div., Inc.
Rockleigh, NJ, US
National Medical Care, Medical Products Div., Inc. appears in FDA device records in Rockleigh, NJ. FDA records list 62 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 62
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
Showing 50 of 62FDA records hold 62 510(k) clearances for National Medical Care, Medical Products Div., Inc. between 1985 and 1996. The busiest year on record is 1990, with 27. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 1 |
| 1986 | 7 |
| 1987 | 3 |
| 1988 | 4 |
| 1989 | 7 |
| 1990 | 27 |
| 1992 | 8 |
| 1993 | 1 |
| 1994 | 1 |
| 1995 | 1 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K962081 | COMBILINES HEMODIALYSIS BLOOD TUBING SET | FJK | Substantially Equivalent | |
| K941757 | FORMALIN REUSE CART | LIF | Substantially Equivalent | |
| K952343 | FOCUA 90R, 90HR, 120R, 120HR, 160R, 160HR HOLLOW FIBER DIALYZER | FJI | Substantially Equivalent | |
| K930843 | RAPID DISCONNECT Y-SET, CAT. NO. 48-7000 | KDJ | Substantially Equivalent | |
| K914790 | HOLLOW FIBER DIALYZER FOCUS 9OR/90H-R/120R/120H-R | FJI | Substantially Equivalent | |
| K920797 | HEMODIALYSIS BLOOD TUBING SET | FJK | Substantially Equivalent | |
| K920697 | DEXTROLYTE II PERITONEAL DIALYSIS 48-3029-7 CLAMP | FJH | Substantially Equivalent | |
| K920693 | DEXTROLYTE II PERITONEAL DIALYSIS 48-3028-9 | FJG | Substantially Equivalent | |
| K920586 | DEXTROLYTE II PERITONEAL DIALYSIS ADMIN. SET | KDJ | Substantially Equivalent | |
| K920029 | DEXTROLYTE II CAPD TRNSFER SET | KDJ | Substantially Equivalent | |
| K915628 | DEXTROLYTE II PERITONEAL DIALYSIS PUMP | KDJ | Substantially Equivalent | |
| K914363 | PERITONEAL DIALYSIS CYCLER SET | KDI | Substantially Equivalent | |
| K905809 | NMC CYCLER MACHINE | FKX | Substantially Equivalent | |
| K903021 | NEGATIVE PRESSURE ARTERIAL LINE CAT. NO: 03-9630 | FJK | Substantially Equivalent | |
| K902451 | LONG-LIFE Y-SET CAT. NO. 48-6366-8 | KDJ | Substantially Equivalent | |
| K901688 | ARTERIAL/VENOUS BLOODLINES | FJK | Substantially Equivalent | |
| K900018 | HOLLOW FIBER DIALYZER, BIO CARE PS 130 | KDI | Substantially Equivalent | |
| K895992 | CATHETER EXTENSION SET CAT. NO. 48-3027-9 | KDJ | Substantially Equivalent | |
| K895792 | DEXTROLYTE II CAPD TRANSFER SET - NO. 48-4009-6 | KDJ | Substantially Equivalent | |
| K900323 | PERITONEAL DIALYSIS CYCLER SET | KDJ | Substantially Equivalent | |
| K900243 | DEXTROLYTE II, PERITONEAL DIALYSIS NO. 48-1015-6 | KDJ | Substantially Equivalent | |
| K900242 | DEXTROLYTE II, PERITONEAL DIALYSIS NO. 48-1031-3 | KDJ | Substantially Equivalent | |
| K900226 | DEXTROLYTE II, PERITONEAL DIALYSIS NO. 48-1001-6 | KDJ | Substantially Equivalent | |
| K900142 | DEXTROLYTE II, W/5 PRONG MANIFOLD NO. 48-1003-2 | KDJ | Substantially Equivalent | |
| K900141 | DEXTROLYTE II, W/5 PRONG MANIFOLD NO. 48-1100-6 | KDJ | Substantially Equivalent | |
| K900140 | DEXTROLYTE II, PERITONEAL DIALYSIS CYCLER SET W/3 | KDJ | Substantially Equivalent | |
| K900012 | DEXTROLYTE II, PERITONEAL DIALYSIS CYCLER SET | KDJ | Substantially Equivalent | |
| K900008 | DEXTROLYTE II, PERITONEAL DIALYSIS CYCLER SET | KDJ | Substantially Equivalent | |
| K896600 | DEXTROLYTE II, SINGLE USE Y SET NO. 48-6360-1 | KDJ | Substantially Equivalent | |
| K896599 | DEXTROLYTE II, PERITONEAL DIALYSIS CYCLER SET -(8) | KDJ | Substantially Equivalent | |
| K895991 | PERITONEAL DIALYSIS DRAINAGE SET NO. 48-0025-6 | KDJ | Substantially Equivalent | |
| K895990 | DEXTROLYTE II PERITONEAL DIALYSIS CYCLER SET | KDJ | Substantially Equivalent | |
| K900005 | DEXTROLYTE II, MANUAL ADMINISTRATION SET 48-1032-1 | KDJ | Substantially Equivalent | |
| K900006 | CATHETER ADAPTER SEALING CAP NO. 48-1028-9 | KDJ | Substantially Equivalent | |
| K900004 | CONVERTIBLE ADAPTER CATALOG NO. 48-4039-3 | KDJ | Substantially Equivalent | |
| K896956 | QUICK DISCONNECT CLAMP CATALOG NO. 48-0300-3 | KDJ | Substantially Equivalent | |
| K896764 | UNIVERSAL CONNECTOR CATALOG NO. 48-1025-5 | KDJ | Substantially Equivalent | |
| K896763 | CATHETER ADAPTER CO-PAK CATALOG NO. 48-0122-1 | KDJ | Substantially Equivalent | |
| K896761 | TRANSFER SET SEALING CAP, CAT. NO. 48-1027-1 | KDJ | Substantially Equivalent | |
| K895244 | MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD. | KOC | Substantially Equivalent | |
| K895759 | HOLLOW FIBER DIALYZER SERIES FOCUS 160/160H | KDI | Substantially Equivalent | |
| K894637 | NATIONAL MEDICAL CARE VENOUS LINE 03-9548 | KOC | Substantially Equivalent | |
| K893677 | HOLLOW FIBER DIALYZER FOCUS 70H | FJI | Substantially Equivalent | |
| K893612 | TWO TANK DISSOLUTION MODULE | FKQ | Substantially Equivalent | |
| K892872 | PERITONEAL DIALYSIS CYCLER SET W/12 PRONG MANIFOLD | KDJ | Substantially Equivalent | |
| K892871 | PERITONEAL DIALYSIS CYCLER SET, W/8 PRONG MANIFOLD | KDJ | Substantially Equivalent | |
| K892870 | PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD | KDJ | Substantially Equivalent | |
| K883408 | NATURALYTE MIXER | FIN | Substantially Equivalent | |
| K883490 | ACCUFLO UF CONTROL MODULE NO. 74-0100-3 | FJB | Substantially Equivalent | |
| K870722 | LABEL CHG FOR ERIKA MODEL 9608 ARTERIAL BLOOD LINE | FJK | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KOCAccessories, Blood Circuit, Hemodialysis
- FJBDetector, Dialysate Level
- LIFDialyzer Reprocessing System
- FJIDialyzer, Capillary, Hollow Fiber
- FJHDialyzer, Disposable
- KDIDialyzer, High Permeability With Or Without Sealed Dialysate System
- FJGDialyzer, Parallel Flow
- FJTIntracatheter, Dialysis
- KDJSet, Administration, For Peritoneal Dialysis, Disposable
- FJKSet, Tubing, Blood, With And Without Anti-Regurgitation Valve
- FKQSystem, Dialysate Delivery, Central Multiple Patient
- FKXSystem, Peritoneal, Automatic Delivery
- FINTank, Holding, Dialysis
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain