Catalog Number

11835

Brand Name

600 KTP Laser Fiber

Version/Model Number

IN-0600S-FT-000-AUR-1

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

-

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

b6af433a-d5d6-47b9-aec8-883b1cb7db64

Public Version Date

May 27, 2021

Public Version Number

1

DI Record Publish Date

May 19, 2021

Package DI Number

00810077635599

Quantity per Package

5

Contains DI Package

00810077630709

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton