Catalog Number

096657

Brand Name

NA

Version/Model Number

Q-940-RT

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

K050738,K050738,K050738

Product Code

GEX

Product Code Name

Powered laser surgical instrument

Public Device Record Key

66a23a74-9c4d-487c-b34d-d86ffbf16568

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

September 28, 2016

Package DI Number

02858028005068

Quantity per Package

2

Contains DI Package

01858028005069

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-