POS-T-VAC AVP-1000 & MVP-700— 510(k) K960342

Substantially Equivalent

Pos-T-Vac, Inc.

FDA 510(k) clearance K960342 for POS-T-VAC AVP-1000 & MVP-700, Substantially Equivalent on 1996-03-01. Applicant: Pos-T-Vac, Inc.. Device class: 2.

Clearance details

Applicant: Pos-T-Vac, Inc.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 1996-01-24
Decision date: 1996-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pos-T-Vac, Inc.

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K012672 — BOSS-2000-2 VACUUM ERECTION DEVICE2001-11-09
K983245 — POS-T-VAC (AVP-1000)1998-11-02

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