Catalog Number

-

Brand Name

HELIOS Ⅲ body

Version/Model Number

HELIOS Ⅲ body

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

K152856,K152856

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

22aee949-df37-474a-96dd-ae038410b559

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 10, 2018

Package DI Number

08800035500092

Quantity per Package

1

Contains DI Package

08800035500009

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton box