Catalog Number

-

Brand Name

RTI

Version/Model Number

19- TABLECLAMP

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 16, 2020

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FWZ

Product Code Name

Operating Room Accessories Table Tray

Public Device Record Key

2d7b9cd6-fe5e-447d-b079-57016f664e15

Public Version Date

June 16, 2020

Public Version Number

4

DI Record Publish Date

December 25, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-