# K060133: Ischemia Albumin Cobalt Binding Test (Acb) Assay Verification Set

- Pathway: 510(k) (Traditional)
- Applicant: Inverness Medical Innovations, Inc.
- Decided: Feb 16, 2006 after 29 days
- Product code: JJX (Single (Specified) Analyte Controls (Assayed And Unassayed))
- Device class: 1
- Regulation: 21 CFR 862.1660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Maine Standards Company VALIDATE CHEM 3 Calibration Verification Test Set: named in the summary without a submission number

## Indications for use
The Ischemia Albumin Cobalt Binding Test (ACB®) Assay Verification Set is intended for use in verifying accuracy of the ACB Test on the Roche Integra 700/800. It is recommended as a part of assay installation. For In Vitro Diagnostic Use

Source page: https://510kreport.com/device/K060133
Methodology: https://510kreport.com/methodology