Brevera Biopsy System with Corlumina Imaging Technology
K-Number: K163052 · 2017-03-29
Device Summary
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.
Related Clinical Trials
Related PubMed Literature
Other Devices by Hologic, Inc.
Related Devices (Code: KNW)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.