• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K101241, REPLENS LONG-LASTING VAGINAL MOISTURIZER (PRE-FILLED APPLICATOR), by Lil Drug Store Products, Inc.

FDA 510(k) K101241, REPLENS LONG-LASTING VAGINAL MOISTURIZER (PRE-FILLED APPLICATOR), by Lil Drug Store Products, Inc.

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510(K) Number: K101241
Device Name: REPLENS LONG-LASTING VAGINAL MOISTURIZER (PRE-FILLED APPLICATOR)
Manufacturer: Lil Drug Store Products, Inc.
Device Classification Name: lubricant, personal
Regulation Number: 884.5300
Classification Product Code: NUC
Date Received: 05/04/2010
Decision Date: 08/17/2010
Regulation Medical Specialty: Obstetrics/Gynecology
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