Catalog Number

-

Brand Name

E.M Adams co, inc.

Version/Model Number

26-0712

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 21, 2021

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)

Yes

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

K971948

Product Code

FMQ

Product Code Name

Restraint, Protective

Public Device Record Key

ce13496f-1b1c-4615-94d4-82e67d1b4856

Public Version Date

June 22, 2021

Public Version Number

2

DI Record Publish Date

December 31, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-