510(k) · Cleared
ClearedVerify Chemical Monitoring Strip for Resert Soultions (Resert XL Test Strip Version 2)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
STERIS Corporation · JOJ Indicator, Physical/Chemical Sterilization Process
Cleared on Feb 9, 2011 as substantially equivalent to K081600 (STERIS Corporation, 2008) after a 180-day review. Its family tree reaches back 3 generations to 1991. 1 later device descends from it.
- Decided
- Feb 9, 2011
- Review
- 180 days
- Class
- Class II
- Product code
- JOJ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K910320 (1991). 5 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 3 generations backK910320 Serim Peracetic Acid Reagent StripsSerim Research Corp. · 1991
- 2 generations backK972035 Sporox Test StripsSerim Research Corp. · 1997
- 1 generation backK081600 Steris Resert XL Test StripSTERIS Corporation · 2008
- This deviceK102296 Verify Chemical Monitoring Strip for Resert Soultions (Resert XL…STERIS Corporation · 2011
- Descendant · cites it directly · 0 of its ownK143333 Revital-Ox RESERT Solution Test StripSTERIS Corporation · 2015
Most influential descendants
Showing 1 of 1 · See all- K143333Revital-Ox RESERT Solution Test StripSTERIS Corporation · 2015 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K910320 | Serim Peracetic Acid Reagent Strips | Serim Research Corp. | 1991 | — |
| −2 | K972035 | Sporox Test Strips | Serim Research Corp. | 1997 | — |
| −1 | K081600 | Steris Resert XL Test Strip | STERIS Corporation | 2008 | — |
| 0 (this device) | K102296 | Verify Chemical Monitoring Strip for Resert Soultions (Resert XL Test Strip… | STERIS Corporation | 2011 | — |
| +1 | K143333 | Revital-Ox RESERT Solution Test Strip | STERIS Corporation | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 1 | 0 |
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in JOJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new JOJ device
- #1 K261992 3M™ Attest™ Steam Chemical Integrator (1243A…score 13.3 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K081600 | Steris Resert XL Test StripSummary page 2…ame: Physical/chemnical sterilization process indicator (21 CFR 880.2800 (b), Product Code JOJ). 2. Predicate Device K08 1600 Verify Chemical Monitoring Strip for Resert Solution (cleared as STERIS Resert XL Test Strip) 3. Description of De… | 2008 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K143333 | Revital-Ox RESERT Solution Test Strip | 2015 | 0 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 20 years and passes through 2 companies; a new generation was cleared every 6.3 years on median.
- 1 of the 5 ancestors has a recall of any class.
- Of its descendants, K143333 (STERIS Corporation, 2015) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K081600.
How does its category compare?
All JOJ devicesJOJ Indicator, Physical/Chemical Sterilization Process: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · JOJ
6in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JOJ
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JOJ
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JOJ
12in 2025
MAUDE reports naming product code JOJ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 8 | 140 | 0 | 1 |
| 2008 | 9 | 57 | 2 | 1 |
| 2009 | 7 | 188 | 2 | 9 |
| 2010 | 6 | 115 | 0 | 3 |
| 2011 | 13 | 151 | 2 | 1 |
| 2012 | 7 | 224 | 0 | 8 |
| 2013 | 6 | 212 | 0 | 6 |
| 2014 | 6 | 198 | 0 | 11 |
| 2015 | 8 | 188 | 0 | 7 |
| 2016 | 4 | 150 | 0 | 11 |
| 2017 | 7 | 172 | 0 | 35 |
| 2018 | 5 | 150 | 0 | 12 |
| 2019 | 12 | 38 | 0 | 8 |
| 2020 | 7 | 108 | 0 | 6 |
| 2021 | 4 | 87 | 1 | 29 |
| 2022 | 8 | 90 | 0 | 23 |
| 2023 | 4 | 53 | 1 | 39 |
| 2024 | 12 | 71 | 0 | 25 |
| 2025 | 6 | 90 | 0 | 12 |
| 2026 | 3 | 30 | 0 | — |
What is it indicated for?
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%.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K102296 · printed Nov 6, 2026
Cite this page
510(k) Report. “K102296: Verify Chemical Monitoring Strip for Resert Soultions (Resert XL Test Strip Version 2).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102296
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026