OKAMOTO CONDOM— 510(k) K952393

Substantially Equivalent

Okamoto USA, Inc.

FDA 510(k) clearance K952393 for OKAMOTO CONDOM, Substantially Equivalent on 1995-08-09. Applicant: Okamoto USA, Inc..

Clearance details

Applicant: Okamoto USA, Inc.
Product code: Code HIS
Advisory panel: Obstetrics/Gynecology
Date received: 1995-05-22
Decision date: 1995-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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