Catalog Number

-

Brand Name

Q-MASTER

Version/Model Number

Q-MASTER

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K172908

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

57e2d127-a15d-42e7-900f-5cbe52d0a1a8

Public Version Date

August 24, 2021

Public Version Number

2

DI Record Publish Date

June 15, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-