Catalog Number

2231

Brand Name

Vas-Q-Clip

Version/Model Number

2231

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

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

K151943,K151943,K151943,K151943,K151943

Product Code

FZP

Product Code Name

CLIP, IMPLANTABLE

Public Device Record Key

91eccc06-a398-4c9e-81f9-502c2ab58322

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

July 01, 2016

Package DI Number

30816537020005

Quantity per Package

3

Contains DI Package

10816537020001

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case