Catalog Number

-

Brand Name

MasterPulse laser fiber 1000 micrometer

Version/Model Number

SU-1000-QRT

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

84c61b7d-eaa2-4f31-bc3d-18ccb291cbd9

Public Version Date

April 07, 2021

Public Version Number

2

DI Record Publish Date

June 18, 2019

Package DI Number

B145118110

Quantity per Package

5

Contains DI Package

B145118090

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton