Catalog Number

2050

Brand Name

Tech-Med

Version/Model Number

2050

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

c980806b-8519-435d-811a-770435406801

Public Version Date

May 23, 2022

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

20665973016966

Quantity per Package

24

Contains DI Package

00665973016962

Package Discontinue Date

May 09, 2018

Package Status

Not in Commercial Distribution

Package Type

Case