Catalog Number

-

Brand Name

Wall bracket, single

Version/Model Number

077.0523

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K130123,K130123

Product Code

BTA

Product Code Name

Pump, Portable, Aspiration (Manual Or Powered)

Public Device Record Key

0b6ac1fb-c2e2-4b59-a51e-290eb8a16776

Public Version Date

March 22, 2022

Public Version Number

4

DI Record Publish Date

December 05, 2016

Package DI Number

07612367003612

Quantity per Package

20

Contains DI Package

07612367051484

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-