Catalog Number

-

Brand Name

Dowell Dental Products, Inc

Version/Model Number

MS1010B

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

EMK

Product Code Name

Curette, Surgical, Dental

Public Device Record Key

aa523811-31c2-4276-90d3-ba2e5685e761

Public Version Date

September 07, 2022

Public Version Number

1

DI Record Publish Date

August 30, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-