Catalog Number

KTP-600

Brand Name

600 micrometer fiber

Version/Model Number

116390

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K022338

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

a3cd8bf6-b69f-4062-89bb-7c6d31ef94cc

Public Version Date

April 07, 2021

Public Version Number

3

DI Record Publish Date

June 28, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-