Cd Medical, Inc.
Miami Lakes, FL, US
Cd Medical, Inc. appears in FDA device records in Miami Lakes, FL. FDA records list 11 510(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
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Cd Medical, Inc. between 1985 and 1994. The busiest year on record is 1985, with 2. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 2 |
| 1986 | 1 |
| 1987 | 2 |
| 1988 | 2 |
| 1989 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K925654 | CD HOME DIALYSERVICE HEMODIALYSIS TRAY | KOC | Unknown | |
| K910215 | DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYST | FKP | Substantially Equivalent | |
| K901520 | WURTZ CHOLEY CLIP (TM) | GBZ | Substantially Equivalent | |
| K894106 | DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST | FIP | Substantially Equivalent | |
| K884353 | ULTRX(TM) 850 ARTIFICIAL KIDNEY | KDI | Substantially Equivalent | |
| K880459 | 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE | FKP | Substantially Equivalent | |
| K873279 | 8810 PUMP-PUMP SINGLE NEEDLE DEVICE | FIF | Substantially Equivalent | |
| K864784 | SERAFLO(TM) BLOODLINES FOR HEMODIALYSIS | FJK | Substantially Equivalent | |
| K862304 | DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM | FKQ | Substantially Equivalent | |
| K853513 | DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY | FKP | Substantially Equivalent | |
| K844185 | MODIFIED C-DAK | KOC | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KOCAccessories, Blood Circuit, Hemodialysis
- GBZCatheter, Cholangiography
- KDIDialyzer, High Permeability With Or Without Sealed Dialysate System
- FIFSet, Dialysis, Single Needle With Uni-Directional Pump
- FJKSet, Tubing, Blood, With And Without Anti-Regurgitation Valve
- FIPSubsystem, Water Purification
- FKQSystem, Dialysate Delivery, Central Multiple Patient
- FKPSystem, Dialysate Delivery, Single Patient
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