CORINNE MCCORMACK INC. - FGX INTERNATIONAL INC.

Duns Number:062312087

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More Product Details

Catalog Number

-

Brand Name

CORINNE MCCORMACK INC.

Version/Model Number

81680.CMC

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

HOI

Product Code Name

Spectacle, magnifying

Device Record Status

Public Device Record Key

d531acb0-6980-4b81-bf8e-e370de419c48

Public Version Date

February 07, 2022

Public Version Number

1

DI Record Publish Date

January 30, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FGX INTERNATIONAL INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 74463