PROMED BIOPSY NEEDLE— 510(k) K933364

Substantially Equivalent

Vlv Associates, Inc.

FDA 510(k) clearance K933364 for PROMED BIOPSY NEEDLE, Substantially Equivalent on 1994-02-15. Applicant: Vlv Associates, Inc.. Device class: 1.

Clearance details

Applicant: Vlv Associates, Inc.
Product code: Code DWO
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1993-07-09
Decision date: 1994-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Hanover, NJ, US

Download summary PDF View on FDA.gov ↗

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More clearances from Vlv Associates, Inc.

K972957 — SA-EF MULTI-LUMEN EXTENSION SET1997-09-29
K964876 — SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET1997-02-28
K955783 — VLV SA.EF INFUSION PORT EXTENSION SETS1996-02-07
K953791 — VLV SA EF INFUSION PORT1995-10-30
K945592 — VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE1995-07-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.