Catalog Number

FS90000

Brand Name

Alpha

Version/Model Number

FS90000

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

K183307

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

8f191142-ee9e-4fd3-8bb5-dab0b23dbeaf

Public Version Date

January 16, 2019

Public Version Number

1

DI Record Publish Date

December 16, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-