Catalog Number

20-1030KI

Brand Name

Symmetry Olsen

Version/Model Number

20-1030KI

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

-

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

02fbd81c-d4b8-41de-b75b-ba812a3c0811

Public Version Date

October 25, 2021

Public Version Number

4

DI Record Publish Date

September 09, 2016

Package DI Number

30841785102685

Quantity per Package

10

Contains DI Package

00841785102684

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-