Catalog Number

8001-061-660

Brand Name

Rapr Round

Version/Model Number

8001-061-660

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K152266,K152266

Product Code

DWJ

Product Code Name

System, thermal regulating

Public Device Record Key

345ba463-ed60-4ef0-b00b-8a8422b559ee

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 16, 2016

Package DI Number

57613327261405

Quantity per Package

5

Contains DI Package

07613327261400

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case