Brevera Breast Biopsy System - Hologic, Inc.

Duns Number:018925968

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More Product Details

Catalog Number

BREVSTXKITG

Brand Name

Brevera Breast Biopsy System

Version/Model Number

BREVSTXKITG

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Unsafe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K163052

Product Code Details

Product Code

KNW

Product Code Name

INSTRUMENT, BIOPSY

Device Record Status

Public Device Record Key

64f5fbe2-d61e-4818-a6df-fff239bce0f7

Public Version Date

September 28, 2018

Public Version Number

1

DI Record Publish Date

August 28, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HOLOGIC, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 130
2 A medical device with a moderate to high risk that requires special controls. 311
3 A medical device with high risk that requires premarket approval 96