Catalog Number

7090

Brand Name

Tissue-Tek AutoTEC® a120

Version/Model Number

7090

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

-

Product Code

IDW

Product Code Name

DISPENSERS, PARAFFIN

Public Device Record Key

0cd9860b-ef96-497a-933b-1486ced0c7e3

Public Version Date

December 04, 2020

Public Version Number

2

DI Record Publish Date

February 06, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-