Vlv Associates, Inc.
Vlv Associates, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1997.
Top product codes for Vlv Associates, Inc.
Recent clearances by Vlv Associates, Inc.
- K972957 — SA-EF MULTI-LUMEN EXTENSION SET
- K964876 — SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET
- K955783 — VLV SA.EF INFUSION PORT EXTENSION SETS
- K953791 — VLV SA EF INFUSION PORT
- K945592 — VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE
- K940406 — DISPOSABLE, AMBULATORY, INFUSION PUMPS
- K933364 — PROMED BIOPSY NEEDLE
- K922469 — PRO-LOK EXTENSION SET(S)
- K904217 — PRO-LOK (TM) EXTENSION SETS
- K901046 — VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR
- K901081 — PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY
- K860071 — HOLD-IT FRAMED ADHESIVE FILM
Data sourced from openFDA. This site is unofficial and independent of the FDA.