KING KONDOM (CONDOM)— 510(k) K882009

Name: FDA 510(k) clearance K882009
Creator: U.S. Food and Drug Administration
Published: 1988-09-21

Substantially Equivalent

King Kondom Products, Inc.

FDA 510(k) clearance K882009 for KING KONDOM (CONDOM), Substantially Equivalent on 1988-09-21. Applicant: King Kondom Products, Inc.. Device class: 2.

Clearance details

Applicant: King Kondom Products, Inc.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1988-05-13
Decision date: 1988-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, CA

Download summary PDF View on FDA.gov ↗

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