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FDA 510(k), K121902, NATRATONE
FDA 510(k), K121902, NATRATONE
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510(K) Number: K121902
Device Name: NATRATONE
Manufacturer: PATRICIA COOMBES
Device Classification Name: Perineometer
Regulation Number: HIR
Classification Product Code: 06/29/2012
Date Received: 06/06/2013
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: NATRATONE
Manufacturer: PATRICIA COOMBES
Device Classification Name: Perineometer
Regulation Number: HIR
Classification Product Code: 06/29/2012
Date Received: 06/06/2013
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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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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