Catalog Number

R-LLF365, R-LLF365-OCS

Brand Name

ProFlex™

Version/Model Number

Reusable 365 Laser Lithotripsy 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

-

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

K142638

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

eaebcdfb-d023-49de-bb63-3db213524523

Public Version Date

April 07, 2021

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-