# Schiff & Co.

- Location (FDA's records): West Cadwell, NJ
- FDA decisions: 15 (1988–1999): 15 510(k) clearances
- Product codes: LYR (2), FRA (2), FOS (1), GMI (1), FPD (1), BTM (1), DTN (1), DHA (1), KHE (1), DZM (1), JQW (1), JKA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Otsuka Pharmaceutical Co., Ltd.: 2 (https://510kreport.com/company/otsuka-pharmaceutical)
- Maquet Cardiopulmonary, AG: 1 (https://510kreport.com/company/maquet-cardiopulmonary)

## Its most-cited devices
- K944159: HM-Cap Eia Kit (1995), cited by 1
- K982136: Jostra Venous Hardshell Cardiotomic Reservoir VHK 4200 (1999), cited by 1
- K955085: HM-Cap Eia Test (Modification) (1996), cited by 1

## Recent decisions
- K990511: X-Tip Intraosseous Perforator (Apr 27, 1999)
- K982136: Jostra Venous Hardshell Cardiotomic Reservoir VHK 4200 (Mar 24, 1999)
- K981629: Nutrisafe Enteral Feeding Tube (Feb 4, 1999)
- K981630: Vygon Double Lumen Umbilical Catheter (Oct 1, 1998)
- K974141: Plus Reusable Resuscitator (May 21, 1998)
- K954448: Viotec V-2200 Ultraviolet Germicidal Air Purification System (Oct 28, 1996)
- K955085: HM-Cap Eia Test (Modification) (Feb 9, 1996)
- K944159: HM-Cap Eia Kit (Jul 18, 1995)

Source page: https://510kreport.com/company/schiff