Catalog Number

-

Brand Name

Duotome Sidelite 550 Fiber

Version/Model Number

Duotome Sidelite 550 Fiber

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

K140388

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

e4b8e370-0f75-42d5-86ec-a784b347072e

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 21, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-