Catalog Number

FNAK10

Brand Name

Aero-Med

Version/Model Number

FNAK10

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

OJT

Product Code Name

Aspiration tray

Public Device Record Key

1c40d911-6754-453a-8fcc-e07461e622f5

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

June 27, 2019

Package DI Number

50810010892114

Quantity per Package

10

Contains DI Package

00810010892119

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE