Catalog Number

ST10

Brand Name

Bovie

Version/Model Number

ST10

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

FTF

Product Code Name

Illuminator, Non-Remote

Public Device Record Key

829eee3d-4899-4391-bce3-e89e813fb07b

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 17, 2016

Package DI Number

10607151069107

Quantity per Package

3

Contains DI Package

00607151069100

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX