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FDA 510(k), K132800, SKINTELL
FDA 510(k), K132800, SKINTELL
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510(K) Number: K132800
Device Name: SKINTELL
Manufacturer: SHAEANN CAVANAGH
Device Classification Name: System, Imaging, Optical Coherence Tomography (Oct)
Regulation Number: NQQ
Classification Product Code: 09/06/2013
Date Received: 03/03/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SKINTELL
Manufacturer: SHAEANN CAVANAGH
Device Classification Name: System, Imaging, Optical Coherence Tomography (Oct)
Regulation Number: NQQ
Classification Product Code: 09/06/2013
Date Received: 03/03/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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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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