BARD INTRAVAGINAL STIM. KIT W/(IVES(TM))— 510(k) K895251

Name: FDA 510(k) clearance K895251
Creator: U.S. Food and Drug Administration
Published: 1989-11-13

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K895251 for BARD INTRAVAGINAL STIM. KIT W/(IVES(TM)), Substantially Equivalent on 1989-11-13. Applicant: C.R. Bard, Inc.. Device class: 2.

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code KPN
Device class: Class 2
Regulation: 21 CFR 876.2040
Advisory panel: Gastroenterology, Urology
Date received: 1989-08-21
Decision date: 1989-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Covington, GA, US

Download summary PDF View on FDA.gov ↗

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