# K102296: Verify Chemical Monitoring Strip for Resert Soultions (Resert XL Test Strip Version 2)

- Pathway: 510(k) (Traditional)
- Applicant: STERIS Corporation
- Decided: Feb 9, 2011 after 180 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: 3 generations back to K910320 (1991). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081600: Steris Resert XL Test Strip, STERIS Corporation (2008) Summary page 2.

## Most influential descendants
- K143333: Revital-Ox RESERT Solution Test Strip (2015), 0 descendants of its own

## Indications for use
The Verify® Chemical Monitoring Strip for Resert Solutions Version 2 is a high level disinfectant concentration monitor dedicated for use with Resert® XL HLD High-Level Disinfectant. The purpose of the Verify® Chemical Monitoring Strip for Resert Solutions Version 2 is to determine whether the concentration of a Resert® XL HLD High-Level Disinfectant solution is above the minimum recommended concentration (MRC) of 1.5%.

Source page: https://510kreport.com/device/K102296
Methodology: https://510kreport.com/methodology