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FDA 510(k)

Brevera Biopsy System with Corlumina Imaging Technology

K-Number: K163052 · 2017-03-29

ApplicantHologic, Inc.
Decision Date2017-03-29
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Brevera Biopsy System with Corlumina Imaging Technology is a medical device manufactured by Hologic, Inc.. It received FDA 510(k) clearance on 2017-03-29 under approval number K163052. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Brevera Biopsy System with Corlumina Imaging Technology?

Brevera Biopsy System with Corlumina Imaging Technology is a medical device that received FDA 510(k) clearance on 2017-03-29. It is manufactured by Hologic, Inc.. The 510(k) number is K163052.

When was Brevera Biopsy System with Corlumina Imaging Technology approved by the FDA?

Brevera Biopsy System with Corlumina Imaging Technology received FDA 510(k) clearance on 2017-03-29, under approval number K163052.

What company makes Brevera Biopsy System with Corlumina Imaging Technology?

Brevera Biopsy System with Corlumina Imaging Technology is manufactured by Hologic, Inc..

What is the FDA product code for Brevera Biopsy System with Corlumina Imaging Technology?

The FDA product code for Brevera Biopsy System with Corlumina Imaging Technology is KNW.

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Official Source

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