Catalog Number

AP-III

Brand Name

HK Aspirator Pump 115V

Version/Model Number

AP-III

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K032802,K032802

Product Code

MUU

Product Code Name

System, Suction, Lipoplasty

Public Device Record Key

cd1181fd-b9ae-44a8-b07a-0bd46241532c

Public Version Date

June 24, 2020

Public Version Number

1

DI Record Publish Date

June 16, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-