FDA 510(k), K920633, PESSARY FLEXIBLE SILICONE NICHOLS
FDA 510(k), K920633, PESSARY FLEXIBLE SILICONE NICHOLS
Device Name: PESSARY FLEXIBLE SILICONE NICHOLS
Manufacturer:
Device Classification Name: Stent, Vaginal
Regulation Number: 884.3900
Classification Product Code: KXP
Date Received: 02/12/1992
Decision Date: 11/08/1995
Regulation Medical Specialty: Obstetrics/Gynecology
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