# K130160: Verify Process Indicator for Reliance Eps

- Pathway: 510(k) (Traditional)
- Applicant: STERIS Corporation
- Decided: Aug 16, 2013 after 205 days
- Product code: JOJ (Indicator, Physical/Chemical Sterilization Process)
- Device class: 2
- Regulation: 21 CFR 880.2800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K043482 (2004). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063285: Reliance CI Process Indicator, Albert Browne, Ltd. (2007) Summary page 3.

## Indications for use
The VERIFY Process Indicator for Reliance Endoscope Processing Systems is intended for routine monitoring of the Reliance Endoscope Processing System (EPS) and the Reliance Advance BPS employing Reliance DG Dry Germicide. The device is a peracetic acid dose indicator that changes color from orange to white (colorless) upon exposure to an effective dose of peracetic acid.

Source page: https://510kreport.com/device/K130160
Methodology: https://510kreport.com/methodology