510(k) Report

510(k) · Cleared

Cleared

VERIFY Chemical Indicator for S40 Sterilant

K173428510(k) TraditionalCleared Mar 2, 2018120-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

STERIS Corporation · JOJ Indicator, Physical/Chemical Sterilization Process

Cleared on Mar 2, 2018 as substantially equivalent to K102217 (STERIS Corporation, 2010) after a 120-day review. Its family tree reaches back 4 generations to 1991. 3 later devices descend from it.

Decided
Mar 2, 2018
Review
120 days
Class
Class II
Product code
JOJ
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K910320 (1991). 8 ancestors in all. 3 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2004: 1 other ancestor2001: 1 other ancestor1994: 1 other ancestor2024: 2 descendants cleared2023: 1 descendant clearedK910320 · Serim Peracetic Acid Reagent Strips · Serim Research Corp. · 1991K972035 · Sporox Test Strips · Serim Research Corp. · 1997K081600 · Steris Resert XL Test Strip · STERIS Corporation · 2008K102217 · System 1E Chemical Indicator · STERIS Corporation · 20101990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors4 generations back: 1 other ancestor 1 generation forward: 2 descendants2 generations forward: 1 descendant K102217 · System 1E Chemical Indicator · STERIS Corporation · 2010K081600 · Steris Resert XL Test Strip · STERIS Corporation · 2008K972035 · Sporox Test Strips · Serim Research Corp. · 1997K910320 · Serim Peracetic Acid Reagent Strips · Serim Research Corp. · 19910
  1. Root · 4 generations backK910320 Serim Peracetic Acid Reagent StripsSerim Research Corp. · 1991
  2. 3 generations backK972035 Sporox Test StripsSerim Research Corp. · 1997
  3. 2 generations backK081600 Steris Resert XL Test StripSTERIS Corporation · 2008
  4. 1 generation backK102217 System 1E Chemical IndicatorSTERIS Corporation · 2010
  5. This deviceK173428 VERIFY Chemical Indicator for S40 SterilantSTERIS Corporation · 2018
  6. Descendant · cites it directly · 1 of its ownK240032 Celerity Chemical Indicator for enspire 3000 CLCSPSSTERIS Corporation · 2024
  7. Descendant · 2 generations on · 0 of its ownK243475 Chemical Indicator for enspire CLCSPS (LCC015)STERIS Corporation · 2024
  8. Descendant · cites it directly · 0 of its ownK233654 VERIFY® Chemical Indicator for SYSTEM 1E® and SYSTEM 1® endo Liquid…Steris · 2023

Most influential descendants

Showing 3 of 3 · See all
  • K240032Celerity Chemical Indicator for enspire 3000 CLCSPSSTERIS Corporation · 2024 · cites it directly1descendant
  • K243475Chemical Indicator for enspire CLCSPS (LCC015)STERIS Corporation · 2024 · 2 generations on0descendants
  • K233654VERIFY® Chemical Indicator for SYSTEM 1E® and SYSTEM 1® endo Liquid Chemical Sterilant…Steris · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K910320Serim Peracetic Acid Reagent StripsSerim Research Corp.1991—
−3K972035Sporox Test StripsSerim Research Corp.1997—
−2K081600Steris Resert XL Test StripSTERIS Corporation2008—
−1K102217System 1E Chemical IndicatorSTERIS Corporation2010—
0 (this device)K173428VERIFY Chemical Indicator for S40 SterilantSTERIS Corporation2018—
+1K240032Celerity Chemical Indicator for enspire 3000 CLCSPSSTERIS Corporation2024—
+2K243475Chemical Indicator for enspire CLCSPS (LCC015)STERIS Corporation2024—
+1K233654VERIFY® Chemical Indicator for SYSTEM 1E® and SYSTEM 1® endo Liquid Chemical…Steris2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
200110
200410
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202420
FIG. 1 — Lineage of K173428, 1991–2024Source: 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
*K102217System 1E Chemical Indicator
Summary page 5
…Physical/chemical sterilization process indicator Classification 21 CFR 880.2800 Product Code JOJ Predicate Device VERIFY® Chemical Indicator for SYSTEM 1E Processor (K102217) Device Description The VERIFY® Chemical Indicator for S40 Sterilant is a single-use chemical indicator consisting of a polypro…
STERIS Corporation2010—

Also cleared against K102217: 1 other device →

What descends from it? (3)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K240032Celerity Chemical Indicator for enspire 3000 CLCSPSSTERIS Corporation20241
K233654VERIFY® Chemical Indicator for SYSTEM 1E® and SYSTEM 1® endo Liquid Chemical Sterilant…Steris20230

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 27 years and passes through 2 companies; a new generation was cleared every 7.3 years on median.
  • 1 of the 8 ancestors has a recall of any class.
  • Of its descendants, K240032 (STERIS Corporation, 2024) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K102217.

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. 2018, 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 VERIFY Chemical Indicator for S40 Sterilant is a peracetic acid concentration indicator for routine monitoring of automated STERIS liquid chemical sterilant processing systems that employ S40 Sterilant Concentrate in a controlled cycle. The unprocessed VERIFY Chemical Indicator for S40 Sterilant is blue. When exposed in a STERIS automated liquid chemical sterilant processor to a concentration of >1820 ppm (mg/L) peracetic acid found in the S40 use…

Read the full statement (112 words)

The VERIFY Chemical Indicator for S40 Sterilant is a peracetic acid concentration indicator for routine monitoring of

automated STERIS liquid chemical sterilant processing systems that employ S40 Sterilant Concentrate in a controlled

cycle.

The unprocessed VERIFY Chemical Indicator for S40 Sterilant is blue. When exposed in a STERIS automated liquid

chemical sterilant processor to a concentration of >1820 ppm (mg/L) peracetic acid found in the S40 use dilution during a

controlled 6-minute exposure at 45.5 — 60°C, the indicator changes color from blue through an intermediate beige and

then to the endpoint color, pink. The indicator may become more pink when exposed to higher peracetic acid

concentrations in S40 sterilant use dilution.

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. “K173428: VERIFY Chemical Indicator for S40 Sterilant.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173428

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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