TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT— 510(k) K000748

Name: FDA 510(k) clearance K000748
Creator: U.S. Food and Drug Administration
Published: 2000-04-06

Substantially Equivalent

Armkel, LLC

FDA 510(k) clearance K000748 for TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT, Substantially Equivalent on 2000-04-06. Applicant: Armkel, LLC. Device class: 2.

Clearance details

Applicant: Armkel, LLC
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 2000-03-08
Decision date: 2000-04-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Cranbury, NJ, 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.