Catalog Number

7210344Y

Brand Name

NA

Version/Model Number

7210344Y

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 04, 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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KQM

Product Code Name

CAMERA, SURGICAL AND ACCESSORIES

Public Device Record Key

89eebdd7-5ac8-4fee-91c1-131ed98b8f5b

Public Version Date

October 24, 2022

Public Version Number

4

DI Record Publish Date

August 29, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-