Catalog Number

130-0071

Brand Name

VASER

Version/Model Number

130-0071

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

-

Product Code

MUU

Product Code Name

System, Suction, Lipoplasty

Public Device Record Key

198d4cde-75c6-4d52-9b8b-39a1db401d2c

Public Version Date

April 02, 2019

Public Version Number

6

DI Record Publish Date

September 23, 2016

Package DI Number

10850608002602

Quantity per Package

10

Contains DI Package

00850608002605

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box