Catalog Number

-

Brand Name

reVive Light Therapy®

Version/Model Number

RVACES

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

46d15ec8-178a-40aa-a892-dfd2ffae8137

Public Version Date

July 07, 2020

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

B347RVACES1

Quantity per Package

24

Contains DI Package

B347RVACES0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-