MODIFIED LABELING ON OKAMOTO HARMONY CONDOM— 510(k) K896339

Substantially Equivalent

Okamoto USA, Inc.

FDA 510(k) clearance K896339 for MODIFIED LABELING ON OKAMOTO HARMONY CONDOM, Substantially Equivalent on 1990-01-10. Applicant: Okamoto USA, Inc..

Clearance details

Applicant: Okamoto USA, Inc.
Product code: Code HIS
Advisory panel: Obstetrics/Gynecology
Date received: 1989-11-03
Decision date: 1990-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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