Catalog Number

2912

Brand Name

Tech-Med

Version/Model Number

2912

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 09, 2018

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K780715,K780715

Product Code

DXQ

Product Code Name

blood pressure cuff

Public Device Record Key

1e9a7dab-70e5-4635-a54e-654f26998bfa

Public Version Date

May 23, 2022

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

20665973016980

Quantity per Package

100

Contains DI Package

00665973016986

Package Discontinue Date

May 09, 2018

Package Status

Not in Commercial Distribution

Package Type

Case