# K062120: Cisbio Renin Ria Test

- Pathway: 510(k) (Traditional)
- Applicant: Cis Bio International
- Decided: Mar 30, 2007 after 248 days
- Product code: CIB (Radioimmunoassay, Angiotensin I And Renin)
- Device class: 2
- Regulation: 21 CFR 862.1085
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
A radioimmunoassay for the quantitative in vitro diagnostic measurement of the level of renin in plasma. Renin measurements are used in the diagnosis and treatment of certain types of hypertension.

Source page: https://510kreport.com/device/K062120
Methodology: https://510kreport.com/methodology