Catalog Number

-

Brand Name

E.M. ADAMS CO, INC

Version/Model Number

EP90487-1

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"

Yes

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,K971948

Product Code

FMQ

Product Code Name

Restraint, Protective

Public Device Record Key

7767ae7c-b5c6-42d6-89b7-15d109506fdc

Public Version Date

July 25, 2022

Public Version Number

1

DI Record Publish Date

July 17, 2022

Package DI Number

50840200324095

Quantity per Package

24

Contains DI Package

10840200324103

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case