Catalog Number

12200000MR

Brand Name

ArcCHECK-MR

Version/Model Number

12200000MR

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K160057

Product Code

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

6f7984a6-1c8a-42a1-aac6-e038528039f0

Public Version Date

June 30, 2020

Public Version Number

2

DI Record Publish Date

May 28, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-