Catalog Number

-

Brand Name

HOMEDICS

Version/Model Number

PX-132CO

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K141105,K141105,K141105,K141105

Product Code

OCH

Product Code Name

Oximeter, Infrared, Sporting, Aviation

Public Device Record Key

3770f6a1-5b1a-444b-8221-e08e4a75c5fd

Public Version Date

November 10, 2021

Public Version Number

3

DI Record Publish Date

July 03, 2020

Package DI Number

10031262099959

Quantity per Package

4

Contains DI Package

20031262099956

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case