Catalog Number

FP8

Brand Name

Ahmed™ Glaucoma Valve

Version/Model Number

FP8

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

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

-

Product Code

KYF

Product Code Name

IMPLANT, EYE VALVE

Public Device Record Key

a5c50132-0374-4c7a-abee-5956de3b82d1

Public Version Date

August 05, 2021

Public Version Number

3

DI Record Publish Date

September 08, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-