Catalog Number

LC 42303

Brand Name

Lipo-One®

Version/Model Number

4mm x 23 cm - 3-hole

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

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

MUU

Product Code Name

System, Suction, Lipoplasty

Public Device Record Key

c913441b-927e-45a9-9f7c-e8218be6994a

Public Version Date

May 01, 2019

Public Version Number

3

DI Record Publish Date

August 13, 2018

Package DI Number

03760037734381

Quantity per Package

6

Contains DI Package

03760037734398

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box