# Vlv Associates, Inc.

- Location (FDA's records): East Hanover, NJ
- FDA decisions: 12 (1986–1997): 12 510(k) clearances
- Product codes: FPA (8), KMK (1), MEB (1), FMF (1), DWO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Pfm Medical, Inc.: 1 (https://510kreport.com/company/pfm-medical)

## Its most-cited devices
- K933364: Promed Biopsy Needle (1994), cited by 1

## Recent decisions
- K972957: SA-EF Multi-Lumen Extension Set (Sep 29, 1997)
- K964876: SA.EF (TM) Infusion Port II - Connector and Extension Set (Feb 28, 1997)
- K955783: VLV SA.EF Infusion Port Extension Sets (Feb 7, 1996)
- K953791: VLV SA EF Infusion Port (Oct 30, 1995)
- K945592: VLV Solodraw (TM) Dual Chamber Piston Syringe (Jul 14, 1995)
- K940406: Disposable, Ambulatory, Infusion Pumps (Sep 2, 1994)
- K933364: Promed Biopsy Needle (Feb 15, 1994)
- K922469: Pro-Lok Extension Set (S) (Mar 15, 1993)

Source page: https://510kreport.com/company/vlv-associates