510(k) Report

510(k) · Cleared

Cleared

DISINTEK™ PA Test Strips

K251035510(k) TraditionalCleared Jun 3, 202561-day reviewClass II21 CFR 880.2800

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Serim Research · JOJ Indicator, Physical/Chemical Sterilization Process

Cleared on Jun 3, 2025 as substantially equivalent to K152394 (Medivators, Inc., 2016) after a 61-day review. Its family tree reaches back 5 generations to 1994.

Decided
Jun 3, 2025
Review
61 days
Class
Class II
Product code
JOJ
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K914145 (1994). 11 ancestors in all, the oldest K931935 (1994). No later device cites it as a predicate yet.

  1. Root · 5 generations backK914145 DSD-91(TM) Disinfector for Flexible EndoscopesMedivators, Inc. · 1994 · Recalled
  2. 4 generations backK040883 Evotech Integrated Endoscope Disinfection SystemAdvanced Sterilization Products · 2005 · Recalled
  3. 3 generations backK061899 Evotech Integrated Endoscope Disinfection SystemAdvanced Sterilization Products · 2006 · Recalled
  4. 2 generations backK082988 Medivators Advantage Plus Endoscope Reprocessing System, Rapicide PA…Medivators Reprocessing Systems · 2009 · Recalled
  5. 1 generation backK152394 Rapicide PA High-Level Disinfectant Test StripsMedivators, Inc. · 2016
  6. This deviceK251035 DISINTEK™ PA Test StripsSerim Research · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K914145DSD-91(TM) Disinfector for Flexible EndoscopesMedivators, Inc.19941
−4K040883Evotech Integrated Endoscope Disinfection SystemAdvanced Sterilization Products20053
−3K061899Evotech Integrated Endoscope Disinfection SystemAdvanced Sterilization Products20062
−2K082988Medivators Advantage Plus Endoscope Reprocessing System, Rapicide PA High…Medivators Reprocessing Systems20094
−1K152394Rapicide PA High-Level Disinfectant Test StripsMedivators, Inc.2016—
0 (this device)K251035DISINTEK™ PA Test StripsSerim Research2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199720
199910
200510
200710
FIG. 1 — Lineage of K251035, 1994–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K261992 3M™ Attest™ Steam Chemical Integrator (1243A…score 13.3 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K152394Rapicide PA High-Level Disinfectant Test Strips
Summary page 5
…ice: MEDIVATORS™ RAPICIDE™ PA Minimum Required Concentration (MRC) Test Strips, REF ML02-0118; K152394. Device Description: The device is a qualitative, single use, reagent chemical i…
Medivators, Inc.2016—

Also cleared against K152394: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 31 years and passes through 4 companies; a new generation was cleared every 7.1 years on median.
  • 4 of the 11 ancestors have a recall of any class.
  • 1 other device also cites its predicate K152394.

How does its category compare?

All JOJ devices

JOJ Indicator, Physical/Chemical Sterilization Process: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · JOJ

6in 2025

2007: 82008: 92009: 72010: 62011: 132012: 72013: 62014: 62015: 82016: 42017: 72018: 52019: 122020: 72021: 42022: 82023: 42024: 122025: 62026 (partial year): 3
2007high 13 (2011) · low 4 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JOJ

90in 2025

2007: 140 days median2008: 57 days median2009: 188 days median2010: 115 days median2011: 151 days median2012: 224 days median2013: 212 days median2014: 198 days median2015: 188 days median2016: 150 days median2017: 172 days median2018: 150 days median2019: 38 days median2020: 108 days median2021: 87 days median2022: 90 days median2023: 53 days median2024: 71 days median2025: 90 days median2026 (partial year): 30 days median
2007high 224 (2012) · low 38 (2019)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · JOJ

1in 2023

2008: 22009: 22011: 22021: 12023: 1
2007high 2 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · JOJ

12in 2025

2007: 12008: 12009: 92010: 32011: 12012: 82013: 62014: 112015: 72016: 112017: 352018: 122019: 82020: 62021: 292022: 232023: 392024: 252025: 12
2007high 39 (2023) · low 1 (2007)2025

MAUDE reports naming product code JOJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007814001
200895721
2009718829
2010611503
20111315121
2012722408
2013621206
20146198011
2015818807
20164150011
20177172035
20185150012
2019123808
2020710806
2021487129
2022890023
2023453139
20241271025
2025690012
20263300—

What is it indicated for?

The Serim™ DISINTEK™ PA Test Strip is a chemical indicator for use in determining whether the concentration of peracetic acid, the active ingredient in the high-level disinfectant RAPICIDE™ PA HLD solution, is above the 850 ppm PAA minimum recommended concentration (MRC) established for RAPICIDE™ PA HLD at both 30°C and 20°C.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K251035: DISINTEK™ PA Test Strips.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K251035

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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