Catalog Number

95-001-216

Brand Name

Ritter

Version/Model Number

95-001-216

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 31, 2018

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

FRK

Product Code Name

CHAIR, EXAMINATION AND TREATMENT

Public Device Record Key

9226e05b-b87e-4526-aa8d-5d3da1b94a1a

Public Version Date

May 05, 2020

Public Version Number

3

DI Record Publish Date

July 28, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-