Catalog Number

-

Brand Name

Debris Collection Bottle for LUS/LUS-2

Version/Model Number

MAJ-1078

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 09, 2022

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

K873367

Product Code

FEO

Product Code Name

Lithotriptor, ultrasonic

Public Device Record Key

cc09c8a3-b260-4dcf-9de6-5caf720d3a1b

Public Version Date

August 22, 2022

Public Version Number

7

DI Record Publish Date

September 21, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-