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FDA 510(k), K163052, Brevera Biopsy System with Corlumina Imaging Technology
FDA 510(k), K163052, Brevera Biopsy System with Corlumina Imaging Technology
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510(K) Number: K163052
Device Name: Brevera Biopsy System with Corlumina Imaging Technology
Manufacturer: HOLOGIC, INC.
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 11/01/2016
Decision Date: 03/29/2017
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: Brevera Biopsy System with Corlumina Imaging Technology
Manufacturer: HOLOGIC, INC.
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 11/01/2016
Decision Date: 03/29/2017
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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