Catalog Number

-

Brand Name

Pastelle

Version/Model Number

Pastelle

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

K123293

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

ded968a4-2784-4e20-92ea-73fdeb5da2ac

Public Version Date

August 24, 2021

Public Version Number

4

DI Record Publish Date

August 16, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-