Catalog Number

012023

Brand Name

AutoSonix

Version/Model Number

012023

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 13, 2019

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

K971861

Product Code

LFL

Product Code Name

Instrument, ultrasonic surgical

Public Device Record Key

8c213112-3e35-4ece-85e2-be98f0d4d222

Public Version Date

August 09, 2021

Public Version Number

2

DI Record Publish Date

August 19, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-