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FDA 510(k), K031463, MARINA MEDICAL SILICONE PESSARY
FDA 510(k), K031463, MARINA MEDICAL SILICONE PESSARY
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510(K) Number: K031463
Device Name: MARINA MEDICAL SILICONE PESSARY
Manufacturer: JAY MANSOUR
Device Classification Name: Pessary, Vaginal
Regulation Number: HHW
Classification Product Code: 05/08/2003
Date Received: 11/18/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: MARINA MEDICAL SILICONE PESSARY
Manufacturer: JAY MANSOUR
Device Classification Name: Pessary, Vaginal
Regulation Number: HHW
Classification Product Code: 05/08/2003
Date Received: 11/18/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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