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FDA 510(k), K132313, PESSARY
FDA 510(k), K132313, PESSARY
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510(K) Number: K132313
Device Name: PESSARY
Manufacturer: EIS CORPORATION
Device Classification Name: pessary, vaginal
Regulation Number: 884.3575
Classification Product Code: HHW
Date Received: 07/25/2013
Decision Date: 12/05/2014
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: PESSARY
Manufacturer: EIS CORPORATION
Device Classification Name: pessary, vaginal
Regulation Number: 884.3575
Classification Product Code: HHW
Date Received: 07/25/2013
Decision Date: 12/05/2014
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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