# Procedure Products, Inc.

- Location (FDA's records): Vancouver, WA
- FDA decisions: 16 (1981–2017): 16 510(k) clearances
- Product codes: FMF (4), DQO (3), FPA (2), DTL (1), HHT (1), DQX (1), FMG (1), DRE (1), HIF (1), KPE (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Dmc Medical, Ltd.: 1 (https://510kreport.com/company/dmc-medical)

## Recent decisions
- K161812: Freedom Syringe (Mar 27, 2017)
- K923194: Insufflator Connecting Filter (Oct 8, 1993)
- K922536: Torque Device (Dec 10, 1992)
- K914128: Connecting Set (Nov 27, 1991)
- K910673: Bag Spigot (Apr 24, 1991)
- K884985: Modified 10CC Syringe Control Ring Set (Dec 20, 1988)
- K874747: 10CC Syringe Control Ring Set (Feb 4, 1988)
- K874037: Angio Waste Fluids Dump Bag (Jan 29, 1988)

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