510(k) Report

510(k) · Cleared

Cleared

Modification to Sterrad Cyclesure Biological Indicator

K071014510(k) SpecialCleared May 24, 200744-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

Advanced Sterilization Products · FRC Indicator, Biological Sterilization Process

Cleared on May 24, 2007 as substantially equivalent to K031226 (Advanced Sterilization Products, 2003) and 1 other predicate after a 44-day review. Its family tree reaches back 2 generations to 2002. 42 later devices descend from it.

Decided
May 24, 2007
Review
44 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K994055 (2002). 42 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 2011: 2 descendants cleared2009: 1 descendant cleared2008: 1 descendant cleared2014: 5 descendants cleared2012: 3 descendants cleared2018: 7 descendants cleared2017: 4 descendants cleared2021: 2 descendants cleared2015: 2 descendants cleared2019: 2 descendants cleared2023: 2 descendants cleared2022: 2 descendants cleared2025: 3 descendants cleared2026: 1 descendant cleared2016: 1 descendant cleared2020: 2 descendants cleared2024: 2 descendants clearedK994055 · Sterrad Cyclesure Biological Indicator · Advanced Sterilization Products · 2002 · recalledK031226 · Sterrad Cyclesure Biological Indicator · Advanced Sterilization Products · 2003 · recalled200020052010201520202025
Descendants, by generation 1 generation forward: 4 descendants2 generations forward: 6 descendants3 generations forward: 6 descendants4 generations forward: 7 descendants5 generations forward: 8 descendants6 generations forward: 5 descendants7 generations forward: 2 descendants8 generations forward: 2 descendants9 generations forward: 1 descendant10 generations forward: 1 descendant K031226 · Sterrad Cyclesure Biological Indicator · Advanced Sterilization Products · 2003 · recalledK994055 · Sterrad Cyclesure Biological Indicator · Advanced Sterilization Products · 2002 · recalled0+5+10
  1. Root · 2 generations backK994055 Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2002 · Recalled
  2. 1 generation backK031226 Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2003 · Recalled
  3. This deviceK071014 Modification to Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2007
  4. Descendant · cites it directly · 20 of its ownK103222 Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2011 · Recalled
  5. Descendant · cites it directly · 20 of its ownK102884 Sterrad Cyclesure 24 Biological IndicatorAdvanced Sterilization Products · 2011
  6. Descendant · cites it directly · 20 of its ownK073244 Verify Self-Contained Biological Indicator for VH202 Gaseous…STERIS Corporation · 2008
  7. Descendant · 2 generations on · 18 of its ownK111375 Sterrad (R) Cyclesure (R) 24 Biological IndicatorAdvanced Sterilization Products · 2012
  8. Descendant · 3 generations on · 17 of its ownK123017 Sterrad Cyclesure 24 Biological Indicator Model 14324Advanced Sterilization Products · 2012

Showing 5 of 42 descendants. See all descendants

Descendants cleared per year

2008: 12009: 12011: 22012: 32014: 52015: 22016: 12017: 42018: 72019: 22020: 22021: 22022: 22023: 22024: 22025: 32026: 1
2008high 7 (2018) · low 0 (2010)2026

Most influential descendants

Showing 5 of 42 · See all
  • K103222Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2011 · cites it directly20descendants
  • K102884Sterrad Cyclesure 24 Biological IndicatorAdvanced Sterilization Products · 2011 · cites it directly20descendants
  • K073244Verify Self-Contained Biological Indicator for VH202 Gaseous Sterilization ProcessesSTERIS Corporation · 2008 · cites it directly20descendants
  • K111375Sterrad (R) Cyclesure (R) 24 Biological IndicatorAdvanced Sterilization Products · 2012 · 2 generations on18descendants
  • K123017Sterrad Cyclesure 24 Biological Indicator Model 14324Advanced Sterilization Products · 2012 · 3 generations on17descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K994055Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products20021
−1K031226Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products20031
0 (this device)K071014Modification to Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products2007—
+1K103222Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products20114
+1K102884Sterrad Cyclesure 24 Biological IndicatorAdvanced Sterilization Products2011—
+1K073244Verify Self-Contained Biological Indicator for VH202 Gaseous Sterilization…STERIS Corporation2008—
+2K111375Sterrad (R) Cyclesure (R) 24 Biological IndicatorAdvanced Sterilization Products2012—
+3K123017Sterrad Cyclesure 24 Biological Indicator Model 14324Advanced Sterilization Products2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
200910
201120
201230
201450
201520
201610
201740
201870
201920
202020
202120
202220
202320
202420
202530
202610
FIG. 1 — Lineage of K071014, 2002–2026Source: 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? (2)

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
*K031226Sterrad Cyclesure Biological Indicator
Summary page 1
…lassification Name: Biological Sterilization Process Indicators 3. Identification of Predicate Device: STERRAD® CycleSure®Biological Indicator, K031226, May 2, 2003 and STERRAD® CycleSure® Biological Indicator, K994055, February 13, 2002 4. Device Descripti…
Advanced Sterilization Products20031
*K994055Sterrad Cyclesure Biological Indicator
Summary page 1
…on of Predicate Device: STERRAD® CycleSure®Biological Indicator, K031226, May 2, 2003 and STERRAD® CycleSure® Biological Indicator, K994055, February 13, 2002 4. Device Description: The STERRAD® CycleSure® Biological Indicator is a self-contained stand-a…
Advanced Sterilization Products20021

Also cleared against K031226: 2 other devices →

What descends from it? (42)

See all 42

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

NumberDeviceApplicantDecidedDescendants
K103222Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products201120
K102884Sterrad Cyclesure 24 Biological IndicatorAdvanced Sterilization Products201120
K073244Verify Self-Contained Biological Indicator for VH202 Gaseous Sterilization ProcessesSTERIS Corporation200820
K090514Verify Self-Contained Biological Indicator for Vaporized (VH2O2) Sterilization ProcessesSTERIS Corporation20094

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 5 years and passes through 1 company; a new generation was cleared every 4.1 years on median.
  • 2 of the 2 ancestors have a recall of any class.
  • Of its descendants, K103222 (Advanced Sterilization Products, 2011) has gone furthest, with 20 descendants of its own.
  • 2 other devices also cite its predicate K031226.

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. 2007, 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 STERRAD® CycleSure® Biological Indicator is intended to be used as a standard method for frequent monitoring of the STERRAD® Sterilizer cycles

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071014: Modification to Sterrad Cyclesure Biological Indicator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K071014

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