Catalog Number

-

Brand Name

Rescue

Version/Model Number

M00538350

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K101298,K101298,K101298

Product Code

OCZ

Product Code Name

Endoscopic Grasping/Cutting Instrument, Non-Powered

Public Device Record Key

8a562b9a-bcb1-4bf2-ba87-f10a35e3d271

Public Version Date

June 21, 2021

Public Version Number

7

DI Record Publish Date

March 01, 2019

Package DI Number

26948318968606

Quantity per Package

5

Contains DI Package

16948318903983

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-