510(k) Report

510(k) · Cleared

Cleared

CELERITY 20 Steam Process Challenge Device for Gravity Cycles

K173629510(k) TraditionalCleared Feb 21, 201889-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 · FRC Indicator, Biological Sterilization Process

Cleared on Feb 21, 2018 as substantially equivalent to K170070 (STERIS Corporation, 2017) after an 89-day review. Its family tree reaches back 5 generations to 1995.

Decided
Feb 21, 2018
Review
89 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K926364 (1995). 9 ancestors in all, the oldest K900771 (1990). No later device cites it as a predicate yet.

  1. Root · 5 generations backK926364 Attest Brand Rapid Readout Biological Ind. #129X3M Health Care, Ltd. · 1995
  2. 4 generations backK090569 Modification to: Attest Rapid Readout Biological Indicator, Mode 12923M Company · 2009
  3. 3 generations backK121484 3M Attest (TM) Super Rapid Readout Biological Indicator, 3M Attest…3M Company · 2012
  4. 2 generations backK121593 3M Attest (TM) Super Radid Readout Steam Challenge Pack 3M Attest…3M Company · 2013
  5. 1 generation backK170070 VERIFY ASSERT STEAM Process Challenge Device for Gravity CyclesSTERIS Corporation · 2017
  6. This deviceK173629 CELERITY 20 Steam Process Challenge Device for Gravity CyclesSTERIS Corporation · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K926364Attest Brand Rapid Readout Biological Ind. #129X3M Health Care, Ltd.1995—
−4K090569Modification to: Attest Rapid Readout Biological Indicator, Mode 12923M Company2009—
−3K1214843M Attest (TM) Super Rapid Readout Biological Indicator, 3M Attest (TM)…3M Company2012—
−2K1215933M Attest (TM) Super Radid Readout Steam Challenge Pack 3M Attest (TM) Super…3M Company2013—
−1K170070VERIFY ASSERT STEAM Process Challenge Device for Gravity CyclesSTERIS Corporation2017—
0 (this device)K173629CELERITY 20 Steam Process Challenge Device for Gravity CyclesSTERIS Corporation2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199410
200210
201110
FIG. 1 — Lineage of K173629, 1995–2018Source: 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 FRC? 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 FRC device

  1. #1 K250044 Celerity 5 HP Biological Indicator (LCB052)…score 14.5 · 10 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
*K170070VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles
Summary page 5
…on Process Indicator (21 CFR 880.2800, FRC) 2. Predicate Device VERIFY Assert STEAM Process Challenge Device for Gravity Cycles, K170070 3. Description of Device Celerity 20 Steam Process Challenge Device for Gravity Cycles (PCD), contains a Celerit…
STERIS Corporation2017—

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 23 years and passes through 3 companies; a new generation was cleared every 3.5 years on median.
  • 1 of the 9 ancestors has a recall of any class.

How does its category compare?

All FRC devices

FRC Indicator, Biological 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 · FRC

6in 2025

2007: 32008: 12009: 62010: 42011: 62012: 92013: 42014: 132015: 32016: 22017: 102018: 182019: 52020: 102021: 52022: 52023: 62024: 82025: 62026 (partial year): 1
2007high 18 (2018) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRC

29in 2025

2007: 83 days median2009: 183 days median2010: 165 days median2011: 118 days median2012: 178 days median2013: 260 days median2014: 174 days median2015: 130 days median2017: 130 days median2018: 97 days median2019: 88 days median2020: 150 days median2021: 107 days median2022: 193 days median2023: 190 days median2024: 105 days median2025: 29 days median
2007high 260 (2013) · low 29 (2025)2026

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

Recalls per year · FRC

8so far in 2026, the most since 2007

2009: 12012: 22013: 22022: 42023: 12026 (partial year): 8
2007high 8 (2026) · low 0 (2007)2026

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

Adverse event reports per year · FRC

9in 2025

2007: 1002008: 602009: 452010: 572011: 372012: 462013: 392014: 512015: 1822016: 4822017: 1822018: 222019: 302020: 162021: 102022: 92023: 202024: 222025: 9
2007high 482 (2016) · low 9 (2022)2025

MAUDE reports naming product code FRC, 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
20073830100
20081—060
20096183145
20104165057
20116118037
20129178246
20134260239
201413174051
201531300182
20162—0482
2017101300182
20181897022
2019588030
202010150016
20215107010
2022519349
20236190120
20248105022
202562909
20261—8—

What is it indicated for?

The Celerity 20 Steam Challenge Pack is used for qualification, routine microbial monitoring, and load monitoring of steam sterilizers.

The validated steam sterilization cycles include:

250°F (121°C) 30-minute gravity

270°F (132°C) 15-minute gravity

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. “K173629: CELERITY 20 Steam Process Challenge Device for Gravity Cycles.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173629

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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