HEADFIRST (CONDOM)— 510(k) K874921

Substantially Equivalent

Stual Products, Inc.

FDA 510(k) clearance K874921 for HEADFIRST (CONDOM), Substantially Equivalent on 1988-05-13. Applicant: Stual Products, Inc.. Device class: 2.

Clearance details

Applicant: Stual Products, Inc.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1987-12-03
Decision date: 1988-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lindenhurst, NY, 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.