Catalog Number

-

Brand Name

Flex-IT Retail 022017

Version/Model Number

FLEI0001R02

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 16, 2017

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K071869

Product Code

LIH

Product Code Name

Interferential Current Therapy

Public Device Record Key

4f9d4d2c-464f-49df-93f2-005976ebf588

Public Version Date

February 19, 2021

Public Version Number

7

DI Record Publish Date

May 16, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-