Catalog Number

AA00X

Brand Name

Bovie

Version/Model Number

AA00X

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

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

HQP

Product Code Name

Unit, Cautery, Thermal, Battery-Powered

Public Device Record Key

60b2760b-73e2-4f7e-973e-9da29cb67f4d

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 11, 2016

Package DI Number

10607151008991

Quantity per Package

10

Contains DI Package

00607151008994

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX