Catalog Number

-

Brand Name

Orfit Industries

Version/Model Number

35779/2MA/EM

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K991319

Product Code

IYE

Product Code Name

Accelerator, linear, medical

Public Device Record Key

6bd5b103-1959-4baf-b52c-853c176099dd

Public Version Date

November 01, 2022

Public Version Number

3

DI Record Publish Date

May 08, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-