Catalog Number

5019

Brand Name

Power Dental USA

Version/Model Number

5019

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"

Yes

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

EMG

Product Code Name

FORCEPS, TOOTH EXTRACTOR, SURGICAL

Public Device Record Key

74fa4f26-33e1-42d1-9c4b-73609d3adc99

Public Version Date

March 24, 2022

Public Version Number

3

DI Record Publish Date

June 20, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-