Catalog Number

-

Brand Name

Premium Plus

Version/Model Number

720C

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

Yes

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

HOY

Product Code Name

Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

Public Device Record Key

60e2f0c9-5d60-4362-abde-8d6004a0d950

Public Version Date

July 07, 2020

Public Version Number

3

DI Record Publish Date

January 08, 2020

Package DI Number

D838720C8

Quantity per Package

50

Contains DI Package

D838720C2

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE