Catalog Number

-

Brand Name

23GA Curved Laser Probe - Iridex

Version/Model Number

PD723.22

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"

Yes

For Single-Use

Yes

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

K024061,K024061

Product Code

GEX

Product Code Name

Powered laser surgical instrument

Public Device Record Key

7c6bb8ff-4562-435a-98f4-6cdbb0b2ab34

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 06, 2016

Package DI Number

10632307000406

Quantity per Package

5

Contains DI Package

00632307000409

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box