510(k) Report

510(k) · Cleared

Cleared

Celerity Incubator

K223715510(k) TraditionalCleared Jun 15, 2023195-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 Jun 15, 2023 as substantially equivalent to K213881 (STERIS Corporation, 2022) after a 195-day review. Its family tree reaches back 5 generations to 2002. 2 later devices descend from it.

Decided
Jun 15, 2023
Review
195 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K004009 (2002). 6 ancestors in all. 2 later devices descend from it, 2 citing it directly.

  1. Root · 5 generations backK004009 3M Attest 290 Auto-Reader3M Company · 2002
  2. 4 generations backK123546 3M Attest (TM) Auto-Reader3M Company · 2013 · Recalled
  3. 3 generations backK171587 VERIFY Incubator for Assert VH2O2 Self-Contained Biological IndicatorSTERIS Corporation · 2017
  4. 2 generations backK190297 Celerity HP IncubatorSTERIS Corporation · 2019
  5. 1 generation backK213881 Celerity IncubatorSTERIS Corporation · 2022
  6. This deviceK223715 Celerity IncubatorSTERIS Corporation · 2023
  7. Descendant · cites it directly · 0 of its ownK250061 Celerity IncubatorSTERIS Corporation · 2025
  8. Descendant · cites it directly · 0 of its ownK233681 ConFirm 20 Minute IncubatorSTERIS Corporation · 2023

Most influential descendants

Showing 2 of 2 · See all
  • K250061Celerity IncubatorSTERIS Corporation · 2025 · cites it directly0descendants
  • K233681ConFirm 20 Minute IncubatorSTERIS Corporation · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K0040093M Attest 290 Auto-Reader3M Company2002—
−4K1235463M Attest (TM) Auto-Reader3M Company20131
−3K171587VERIFY Incubator for Assert VH2O2 Self-Contained Biological IndicatorSTERIS Corporation2017—
−2K190297Celerity HP IncubatorSTERIS Corporation2019—
−1K213881Celerity IncubatorSTERIS Corporation2022—
0 (this device)K223715Celerity IncubatorSTERIS Corporation2023—
+1K250061Celerity IncubatorSTERIS Corporation2025—
+1K233681ConFirm 20 Minute IncubatorSTERIS Corporation2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202510
FIG. 1 — Lineage of K223715, 2002–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K213881Celerity Incubator
Summary page 5
…or, Biological Sterilization Process Classification Number: 21 CFR 880.2800 Product Code: FRC 2. Predicate Device K213881 – Celerity Incubator 3. Device Description The Celerity Incubator incubates and reads fluorescent Vaporized Hydrogen…
STERIS Corporation2022—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K250061Celerity IncubatorSTERIS Corporation20250
K233681ConFirm 20 Minute IncubatorSTERIS Corporation20230

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 21 years and passes through 2 companies; a new generation was cleared every 3.2 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K250061 (STERIS Corporation, 2025) has gone furthest, with 0 descendants of its own.

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. 2023, 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?

Use the Celerity Incubator to incubate and automatically read STERIS Celerity Biological Indicators for Steam and Vaporized Hydrogen Peroxide sterilization at 55 ° C - 60 ° C for a fluorescent result.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K223715: Celerity Incubator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K223715

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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