Catalog Number

-

Brand Name

N.A.

Version/Model Number

774-231-00

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 09, 2022

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

Yes

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

-

Product Code

ECI

Product Code Name

BAND, ELASTIC, ORTHODONTIC

Public Device Record Key

1247e264-2114-4619-b9ab-92a89b54987f

Public Version Date

April 11, 2022

Public Version Number

4

DI Record Publish Date

September 15, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-