APOLLO CONDOM— 510(k) K874236

Substantially Equivalent

Apollo Enterprise, Ltd. Co.

FDA 510(k) clearance K874236 for APOLLO CONDOM, Substantially Equivalent on 1988-07-01. Applicant: Apollo Enterprise, Ltd. Co.. Device class: 2.

Clearance details

Applicant: Apollo Enterprise, Ltd. Co.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1987-10-15
Decision date: 1988-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, 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.