510(k) Report

510(k) · Cleared

Recalled · Class II · 2013

Amsco Chimeron Medium Steam Sterlilzer

K112403510(k) AbbreviatedCleared May 8, 2012260-day reviewClass II21 CFR 880.6880Recalls 1

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

STERIS Corporation · FLE Sterilizer, Steam

Cleared on May 8, 2012 as substantially equivalent to K020747 (STERIS Corporation, 2002) after a 260-day review. Its family tree reaches back 2 generations to 2001. 7 later devices descend from it. It has been recalled once.

Decided
May 8, 2012
Review
260 days
Class
Class II
Product code
FLE
Recalls
1
Predicates
1

Its longest line of descent runs back 2 generations to K010865 (2001). 7 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2019: 1 descendant cleared2021: 2 descendants cleared2022: 3 descendants cleared2023: 1 descendant clearedK010865 · Amsco Century Medium Sterilizer, Model Century · STERIS Corporation · 2001 · recalledK020747 · Amsco Century Medium Sterilizer 26 X 26 · STERIS Corporation · 2002200020052010201520202025
Descendants, by generation 1 generation forward: 2 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant4 generations forward: 1 descendant K020747 · Amsco Century Medium Sterilizer 26 X 26 · STERIS Corporation · 2002K010865 · Amsco Century Medium Sterilizer, Model Century · STERIS Corporation · 2001 · recalled0
  1. Root · 2 generations backK010865 Amsco Century Medium Sterilizer, Model CenturySTERIS Corporation · 2001 · Recalled
  2. 1 generation backK020747 Amsco Century Medium Sterilizer 26 X 26STERIS Corporation · 2002
  3. This deviceK112403 Amsco Chimeron Medium Steam SterlilzerSTERIS Corporation · 2012
  4. Descendant · cites it directly · 5 of its ownK183410 AMSCO 600 Steam SterilizerSTERIS Corporation · 2019
  5. Descendant · 2 generations on · 2 of its ownK211500 AMSCO 600 Medium Steam SterilizerSTERIS Corporation · 2021
  6. Descendant · 3 generations on · 1 of its ownK222543 AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature…Steris · 2022
  7. Descendant · 2 generations on · 0 of its ownK213545 Steelco VS Series Steam Sterilizers, models 262839, 262851, 262869Steelco S.P.A. · 2023
  8. Descendant · 4 generations on · 0 of its ownK222849 AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature…Steris · 2022

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2019: 12021: 22022: 32023: 1
2019high 3 (2022) · low 0 (2020)2026

Most influential descendants

Showing 5 of 7 · See all
  • K183410AMSCO 600 Steam SterilizerSTERIS Corporation · 2019 · cites it directly5descendants
  • K211500AMSCO 600 Medium Steam SterilizerSTERIS Corporation · 2021 · 2 generations on2descendants
  • K222543AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature Sterilization System, V-PRO s2…Steris · 2022 · 3 generations on1descendant
  • K213545Steelco VS Series Steam Sterilizers, models 262839, 262851, 262869Steelco S.P.A. · 2023 · 2 generations on0descendants
  • K222849AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature Sterilization System, V-PRO s2…Steris · 2022 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K010865Amsco Century Medium Sterilizer, Model CenturySTERIS Corporation20011
−1K020747Amsco Century Medium Sterilizer 26 X 26STERIS Corporation2002—
0 (this device)K112403Amsco Chimeron Medium Steam SterlilzerSTERIS Corporation2012—
+1K183410AMSCO 600 Steam SterilizerSTERIS Corporation2019—
+2K211500AMSCO 600 Medium Steam SterilizerSTERIS Corporation2021—
+3K222543AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature Sterilization System…Steris2022—
+2K213545Steelco VS Series Steam Sterilizers, models 262839, 262851, 262869Steelco S.P.A.2023—
+4K222849AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature Sterilization System…Steris2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202120
202230
202310
FIG. 1 — Lineage of K112403, 2001–2023Source: 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 FLE? 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 FLE device

  1. #1 K250168 Life Ultra 25L Tabletop Mono Chamber Steam…score 12.7 · 8 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
*K020747Amsco Century Medium Sterilizer 26 X 26
Summary page 2
…lizer Classification Name: Steam Sterilizer (21 CFR 880.6880) Product Code FLE 2. Predicate Device K020747, AMSCO Century Medium Steam Sterilizer, product code [FLE] cleared May 1 7 Ih, 2002. 3. Description of Device…
STERIS Corporation2002—

Also cleared against K020747: 1 other device →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K183410AMSCO 600 Steam SterilizerSTERIS Corporation20195
K212424AMSCO 400 Small Steam Sterilizers, AMSCO 400 Medium Steam SterilizersSTERIS Corporation20210

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Feb 12, 2013Class IIZ-0915-2013Software designThe control boards alarm set points and temperature tolerances allowed for erroneous activation of the AD (analog/digital) alarm as temperature fluctuated during operation. When this alarm occurs, the sterilizer locks up and cannot be…

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 11 years and passes through 1 company; a new generation was cleared every 10.0 years on median.
  • 1 of the 2 ancestors has a recall of any class.
  • Of its descendants, K183410 (STERIS Corporation, 2019) has gone furthest, with 5 descendants of its own.
  • 1 other device also cites its predicate K020747.

How does its category compare?

All FLE devices

FLE Sterilizer, Steam: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · FLE

4in 2025

2007: 52008: 12009: 82010: 22011: 52012: 52013: 52014: 22015: 32016: 12017: 32018: 82019: 52020: 22021: 52022: 102023: 72024: 22025: 42026 (partial year): 3
2007high 10 (2022) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FLE

184in 2025

2007: 67 days median2009: 109 days median2011: 141 days median2012: 111 days median2013: 241 days median2015: 302 days median2017: 233 days median2018: 146 days median2019: 192 days median2021: 147 days median2022: 133 days median2023: 88 days median2025: 184 days median2026 (partial year): 85 days median
2007high 302 (2015) · low 67 (2007)2026

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

Recalls per year · FLE

1in 2021

2007: 12008: 12011: 12012: 12013: 22015: 12018: 12019: 22021: 12026 (partial year): 1
2007high 2 (2013) · low 0 (2009)2026

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

Adverse event reports per year · FLE

71in 2025

2007: 192008: 212009: 192010: 202011: 632012: 692013: 1122014: 1132015: 682016: 762017: 632018: 902019: 912020: 872021: 812022: 702023: 662024: 642025: 71
2007high 113 (2014) · low 19 (2007)2025

MAUDE reports naming product code FLE, 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
2007567119
20081—121
20098109019
20102—020
20115141163
20125111169
201352412112
20142—0113
20153302168
20161—076
20173233063
20188146190
20195192291
20202—087
20215147181
202210133070
2023788066
20242—064
20254184071
20263851—

What is it indicated for?

The AMSCO Chimeron Medium Steam Sterilizers (Models 39SL and 39CSL) are designed for sterilization of heat and moisture-stable materials used in healthcare facilities and are available in the following configuration:

Prevacuum - equipped with Prevacuum, Gravity, Liquid, Leak Test and DART

(Bowie-Dick) cycles.

The AMSCO Chimeron Medium Prevacuum Steam Sterilizers are equipped with the following factory-programmed sterilization cycles and cycle values (Table A-I):

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112403: Amsco Chimeron Medium Steam Sterlilzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K112403

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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