Catalog Number

-

Brand Name

RITEAID

Version/Model Number

079573101988

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"

-

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

-

Product Code

MVV

Product Code Name

Device, Acupressure

Public Device Record Key

422d10a2-f8e2-4804-8d9c-20346df2039a

Public Version Date

December 13, 2021

Public Version Number

1

DI Record Publish Date

December 03, 2021

Package DI Number

20011822820138

Quantity per Package

12

Contains DI Package

00011822820134

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

INNER