KISS OF MINT(TM) NON-LUBRICATED CONDOM— 510(k) K882389

Name: FDA 510(k) clearance K882389
Creator: U.S. Food and Drug Administration
Published: 1988-10-20

Substantially Equivalent

Ansell, Inc.

FDA 510(k) clearance K882389 for KISS OF MINT(TM) NON-LUBRICATED CONDOM, Substantially Equivalent on 1988-10-20. Applicant: Ansell, Inc.. Device class: 2.

Clearance details

Applicant: Ansell, Inc.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1988-06-10
Decision date: 1988-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dothan, AL, US

Download summary PDF View on FDA.gov ↗

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