Catalog Number

-

Brand Name

HELIOS IV 785 532 FX Handpiece

Version/Model Number

HELIOS IV 785 532 FX Handpiece

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

K212663

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

5309a793-0c2c-4320-9163-43f0a75b3a69

Public Version Date

June 28, 2022

Public Version Number

1

DI Record Publish Date

June 20, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-