Catalog Number

JP1099351

Brand Name

Actiwatch Spectrum Pro

Version/Model Number

Actiwatch Spectrum PRO Japan

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 05, 2021

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

IKK

Product Code Name

SYSTEM, ISOKINETIC TESTING AND EVALUATION

Public Device Record Key

9e1b7a03-3b7e-4287-a0eb-c91678edfe05

Public Version Date

March 05, 2021

Public Version Number

5

DI Record Publish Date

September 19, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-