510(k) Report

510(k) · Cleared

Recalled · Class II · 2023

3M Attest Super Rapid 5 Steam-Plus Challenge Pack

K193154510(k) TraditionalCleared Feb 7, 202085-day reviewClass II21 CFR 880.2800Recalls 2

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

3M Company · FRC Indicator, Biological Sterilization Process

Cleared on Feb 7, 2020 as substantially equivalent to K173519 (3M Company, 2018) after an 85-day review. Its family tree reaches back 5 generations to 1995. 3 later devices descend from it. It has been recalled 2 times.

Decided
Feb 7, 2020
Review
85 days
Class
Class II
Product code
FRC
Recalls
2
Predicates
1

Its longest line of descent runs back 5 generations to K926364 (1995). 9 ancestors in all, the oldest K900771 (1990). 3 later devices descend from it, 3 citing it directly.

  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 backK173519 3M Attest Super Rapid Readout Steam Challenge Pack, 3M Attest Super…3M Company · 2018 · Recalled
  6. This deviceK193154 3M Attest Super Rapid 5 Steam-Plus Challenge Pack3M Company · 2020
  7. Descendant · cites it directly · 0 of its ownK241959 3M™ Attest™ Super Rapid Steam Clear Challenge Pack (1492PCD); 3M™…3M Company · 2024
  8. Descendant · cites it directly · 0 of its ownK200766 3M Attest Steam Chemical Integrator Test Pack3M Company · 2020
  9. Descendant · cites it directly · 0 of its ownK200536 3MTM AttestTM Rapid 5 Steam-Plus Test Pack3M Complany · 2020

Most influential descendants

Showing 3 of 3 · See all
  • K2419593M™ Attest™ Super Rapid Steam Clear Challenge Pack (1492PCD); 3M™ Attest™ Auto-reader…3M Company · 2024 · cites it directly0descendants
  • K2007663M Attest Steam Chemical Integrator Test Pack3M Company · 2020 · cites it directly0descendants
  • K2005363MTM AttestTM Rapid 5 Steam-Plus Test Pack3M Complany · 2020 · cites it directly0descendants
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—
−1K1735193M Attest Super Rapid Readout Steam Challenge Pack, 3M Attest Super Rapid 5…3M Company20181
0 (this device)K1931543M Attest Super Rapid 5 Steam-Plus Challenge Pack3M Company2020—
+1K2419593M™ Attest™ Super Rapid Steam Clear Challenge Pack (1492PCD); 3M™ Attest™…3M Company2024—
+1K2007663M Attest Steam Chemical Integrator Test Pack3M Company2020—
+1K2005363MTM AttestTM Rapid 5 Steam-Plus Test Pack3M Complany2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199410
200210
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202020
202410
FIG. 1 — Lineage of K193154, 1995–2024Source: 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 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
*K1735193M Attest Super Rapid Readout Steam Challenge Pack, 3M Attest Super Rapid 5 Steam-Plus…
Summary page 5
…21 CFR § 880.2800(a), FRC] Predicate Device: 3M™ Attest™ Super Rapid 5 Steam-Plus Challenge Pack 41482V, 3M™ Attest™ Auto-reader 490, and 3M™ Attest™ Auto-reader 490H, K173519 Indications for Use Use 3M™ Attest™ Super Rapid 5 Steam-Plus Challenge Pack 41482V in conjunction with the 3M™ Attest™ Auto-rea…
3M Company20181
†K101249Sterigage Model 1243RA, 1243RB, 1243RE3M Company2010—

Also cleared against K173519: 1 other device →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K2419593M™ Attest™ Super Rapid Steam Clear Challenge Pack (1492PCD); 3M™ Attest™ Auto-reader…3M Company20240
K2007663M Attest Steam Chemical Integrator Test Pack3M Company20200
K2005363MTM AttestTM Rapid 5 Steam-Plus Test Pack3M Complany20200

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

Recalls of this device

DateClassRecallRoot causeReason
Aug 22, 2023Class IIZ-2639-2023Process controlSpecific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam Challenge (1496V) may contain biological indicators with…
Aug 22, 2023Class IIZ-2640-2023Process controlSpecific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam Challenge (1496V) may contain biological indicators with…

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 25 years and passes through 2 companies; a new generation was cleared every 3.5 years on median.
  • 2 of the 9 ancestors have a recall of any class.
  • Of its descendants, K241959 (3M Company, 2024) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K173519.

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. 2020, 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 3M™ Attest™ Super Rapid 5 Steam-Plus Challenge Pack 41482V in conjunction with the 3M™ Attest™ Auto-reader 490 or 3M™ Attest™ Auto-reader 490H having software version 4.0.0 or greater to qualify or monitor dynamic-air-removal steam sterilization cycles of 4 minutes at 270°F (132°C) and 3 minutes at 275°F (135°C).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K193154: 3M Attest Super Rapid 5 Steam-Plus Challenge Pack.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K193154

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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