# Neotech Products, Inc.

- Location (FDA's records): Chatsworth, CA
- FDA decisions: 6 (1988–2002): 6 510(k) clearances
- Product codes: BSY (1), BZA (1), KNX (1), DRX (1), FAQ (1), BTR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Ambu A/S: 1 (https://510kreport.com/company/ambu-a-s)
- R & D Medical Products, Inc.: 1 (https://510kreport.com/company/r-d-medical-products)
- Integral Process Sas: 1 (https://510kreport.com/company/integral-process)
- Kentec Medical, Inc.: 1 (https://510kreport.com/company/kentec-medical)

## Its most-cited devices
- K011564: Neolead (2002), cited by 4

## Recent decisions
- K011564: Neolead (Jan 3, 2002)
- K931727: Urinary Drainage Bag Caddy (Jul 23, 1993)
- K921024: Uro-Tote Leg Bag (Sep 2, 1992)
- K890425: Neotech Mucus Trap W/Catheter (Apr 19, 1989)
- K882203: Neotech Universal Adapter (Jun 17, 1988)
- K880487: Neotech Meconium Aspirator (Sterile) (May 6, 1988)

Source page: https://510kreport.com/company/neotech-products