Catalog Number

-

Brand Name

Equate

Version/Model Number

581880438

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

January 06, 2030

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"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K172925,K172925

Product Code

LRX

Product Code Name

Case, Contact Lens

Public Device Record Key

15e02071-1e07-42e0-8977-a588549518f9

Public Version Date

January 15, 2021

Public Version Number

1

DI Record Publish Date

January 07, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-