Catalog Number

-

Brand Name

LF

Version/Model Number

700539

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 11, 2019

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

K943581

Product Code

IXR

Product Code Name

Table, Radiographic, Tilting

Public Device Record Key

c7946564-15c1-4f9a-ada3-8f404de49ae5

Public Version Date

January 05, 2022

Public Version Number

6

DI Record Publish Date

September 09, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-