Catalog Number

-

Brand Name

COOLEY SUBRAMANIAN AORTIC CLAMP

Version/Model Number

2100-145

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

-

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

K092544

Product Code

DXC

Product Code Name

Clamp, Vascular

Public Device Record Key

8d7bbc9b-dffc-481d-a572-8fb5cc1c8dfd

Public Version Date

August 21, 2019

Public Version Number

3

DI Record Publish Date

August 22, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-