Catalog Number

FT0022W

Brand Name

ForceTriad

Version/Model Number

FT0022W

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

-

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

K110268,K110268

Product Code

GEI

Product Code Name

ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Public Device Record Key

8dcec495-8d76-46ba-9785-e9c13d9fdc73

Public Version Date

November 23, 2018

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

10884521062092

Quantity per Package

20

Contains DI Package

20884521062099

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE