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FDA 510(k) K021737, REPHRESH VAGINAL GEL, by Columbia Laboratories, Inc.

FDA 510(k) K021737, REPHRESH VAGINAL GEL, by Columbia Laboratories, Inc.

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510(K) Number: K021737
Device Name: REPHRESH VAGINAL GEL
Manufacturer: Columbia Laboratories, Inc.
Device Classification Name: Lubricant, Personal
Regulation Number: 884.5300
Classification Product Code: NUC
Date Received: 05/28/2002
Decision Date: 08/26/2002
Regulation Medical Specialty: Obstetrics/Gynecology
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