Catalog Number

-

Brand Name

Surgeon's Preference

Version/Model Number

T-500

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

K864402,K864402,K864402

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

82b415fe-bbc3-4fb1-93f0-7f2d6ad33c59

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

July 04, 2016

Package DI Number

20841019110045

Quantity per Package

50

Contains DI Package

00841019110041

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-