Schiff & Co.
West Cadwell, NJ, US
Schiff & Co. appears in FDA device records in West Cadwell, NJ. FDA records list 15 510(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
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Schiff & Co. between 1988 and 1999. The busiest year on record is 1988, with 3. The most recent is 1999, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 3 |
| 1989 | 2 |
| 1990 | 1 |
| 1995 | 2 |
| 1996 | 2 |
| 1998 | 2 |
| 1999 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K990511 | X-TIP INTRAOSSEOUS PERFORATOR | DZM | Substantially Equivalent | |
| K982136 | JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 | DTN | Substantially Equivalent | |
| K981629 | NUTRISAFE ENTERAL FEEDING TUBE | FPD | Substantially Equivalent | |
| K981630 | VYGON DOUBLE LUMEN UMBILICAL CATHETER | FOS | Substantially Equivalent | |
| K974141 | PLUS REUSABLE RESUSCITATOR | BTM | Substantially Equivalent | |
| K954448 | VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM | FRA | Substantially Equivalent | |
| K955085 | HM-CAP EIA TEST (MODIFICATION) | LYR | Substantially Equivalent | |
| K944159 | HM-CAP EIA KIT | LYR | Substantially Equivalent | |
| K943521 | VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE | FRA | Substantially Equivalent | |
| K896684 | KEMBLE LIQUID HANDLING SYSTEM DISPENSER | JQW | Substantially Equivalent | |
| K894617 | OLYMPUS PK-TP SYSTEM REACTIVE CONTROL | GMI | Substantially Equivalent | |
| K895967 | FASTEC 901 AGGLUTINATION PATTERN READER | JJQ | Substantially Equivalent | |
| K882539 | CLEANTECH SYSTEM | JKA | Substantially Equivalent | |
| K874482 | REVISED IMMUDIA HEM-SP | KHE | Substantially Equivalent | |
| K873986 | BETA-HCG ASSAY | DHA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GMIAntigen, Cf And / Or Id, Coccidioides Immitis
- FOSCatheter, Umbilical Artery
- JJQColorimeter, Photometer, Spectrophotometer For Clinical Use
- LYRHelicobacter Pylori
- DZMNeedle, Dental
- FRAPurifier, Air, Ultraviolet, Medical
- KHEReagent, Occult Blood
- DTNReservoir, Blood, Cardiopulmonary Bypass
- JQWStation, Pipetting And Diluting, For Clinical Use
- DHASystem, Test, Human Chorionic Gonadotropin
- FPDTube, Feeding
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
- BTMVentilator, Emergency, Manual (Resuscitator)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain