Catalog Number

SA2016

Brand Name

ACE

Version/Model Number

SA2016

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

K113374

Product Code

CEO

Product Code Name

Phosphomolybdate (Colorimetric), Inorganic Phosphorus

Public Device Record Key

0126a555-007c-4625-98e7-4910d5ac0f9b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 10, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-