FDA 510(k), K094039, HYALO GYN

FDA 510(k), K094039, HYALO GYN

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510(K) Number: K094039
Device Name: HYALO GYN
Manufacturer: GIUSI LOCASTRO
Device Classification Name: Lubricant, Personal
Regulation Number: NUC
Classification Product Code: 12/30/2009
Date Received: 05/07/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
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