Catalog Number

0200

Brand Name

QuikClot

Version/Model Number

0200

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

Yes

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

K072474,K072474

Product Code

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

547ffc6d-3c38-48f6-8abe-965bd92f2f95

Public Version Date

February 21, 2022

Public Version Number

5

DI Record Publish Date

February 10, 2021

Package DI Number

50841495102009

Quantity per Package

50

Contains DI Package

00841495102004

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper