KNIGHT LIGHT NONLUBRICATED CONDOM— 510(k) K960552

Name: FDA 510(k) clearance K960552
Creator: U.S. Food and Drug Administration
Published: 1997-11-20

Substantially Equivalent

Global Protection Corp.

FDA 510(k) clearance K960552 for KNIGHT LIGHT NONLUBRICATED CONDOM, Substantially Equivalent on 1997-11-20. Applicant: Global Protection Corp.. Device class: 2.

Clearance details

Applicant: Global Protection Corp.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1996-02-08
Decision date: 1997-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, 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.