Catalog Number

A-23013P

Brand Name

Core-Flo DC DualSyr Blue Pkg

Version/Model Number

A-23013P

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 19, 2018

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

-

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

EBF

Product Code Name

MATERIAL, TOOTH SHADE, RESIN

Public Device Record Key

91e2e45b-237a-40d1-bf0e-73bec58f4c1f

Public Version Date

June 20, 2018

Public Version Number

3

DI Record Publish Date

June 12, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-