Catalog Number

LC 32302

Brand Name

Lipo-One®

Version/Model Number

3mm x 23 cm - 2-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

916e29af-45cc-47dd-a639-70011b44e1f0

Public Version Date

May 01, 2019

Public Version Number

3

DI Record Publish Date

August 13, 2018

Package DI Number

03760037734268

Quantity per Package

6

Contains DI Package

03760037734275

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box