Catalog Number

R-LLF550-T-USL

Brand Name

ProFlex™

Version/Model Number

550 Reusable Laser Lithotripsy Fiber var. Trimedyne

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

K180140

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

43365a30-be46-4f0b-ab49-e3aeb7a44a59

Public Version Date

April 07, 2021

Public Version Number

2

DI Record Publish Date

August 18, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-