Catalog Number

-

Brand Name

Dosimetry Check

Version/Model Number

4

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K010225,K101503,K132605

Product Code

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

a39a813c-a27c-47c3-b0ae-634793e4d516

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

June 17, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-