FDA 510(k), K974479, SILIMED VAGINAL STENT
FDA 510(k), K974479, SILIMED VAGINAL STENT
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510(K) Number: K974479
Device Name: SILIMED VAGINAL STENT
Manufacturer:
Device Classification Name: Stent, Vaginal
Regulation Number: 884.3900
Classification Product Code: KXP
Date Received: 11/26/1997
Decision Date: 08/05/1998
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: SILIMED VAGINAL STENT
Manufacturer:
Device Classification Name: Stent, Vaginal
Regulation Number: 884.3900
Classification Product Code: KXP
Date Received: 11/26/1997
Decision Date: 08/05/1998
Regulation Medical Specialty: Obstetrics/Gynecology