Catalog Number

-

Brand Name

PROBE 418 Master Probe

Version/Model Number

PROBE 418

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 04, 2021

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K935495

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

1f171efc-72c2-4aab-94e9-004efae43ef1

Public Version Date

October 05, 2021

Public Version Number

4

DI Record Publish Date

September 13, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-