510(k) Report

510(k) · Cleared

Cleared

3MTM AttestTM Super Rapid Steam Biological Indicator 1592, 3MTM AttestTM Super Rapid Steam Challenge Pack, 3MTM AttestTM Auto- Readers 490 and 490H

K192550510(k) TraditionalCleared Jun 5, 2020262-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

3M Company · FRC Indicator, Biological Sterilization Process

Cleared on Jun 5, 2020 as substantially equivalent to K173437 (3M Company, 2018) and 1 other predicate after a 262-day review. Its family tree reaches back 5 generations to 1995. 2 later devices descend from it.

Decided
Jun 5, 2020
Review
262 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K926364 (1995). 10 ancestors in all, the oldest K900771 (1990). 2 later devices descend from it, 1 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 deviceK192550 3MTM AttestTM Super Rapid Steam Biological Indicator 1592, 3MTM…3M Company · 2020
  7. Descendant · cites it directly · 1 of its ownK213809 3M Attest Super Rapid Steam Biological Indicator, 3M Attest Super…3M Company · 2022
  8. Descendant · 2 generations on · 0 of its ownK242538 3M™ Attest™ Super Rapid Readout Biological Indicator 1493; 3M™…3M Company · 2024

Most influential descendants

Showing 2 of 2 · See all
  • K2138093M Attest Super Rapid Steam Biological Indicator, 3M Attest Super Rapid Steam Challenge…3M Company · 2022 · cites it directly1descendant
  • K2425383M™ Attest™ Super Rapid Readout Biological Indicator 1493; 3M™ Attest™ Super Rapid Steam…3M Company · 2024 · 2 generations on0descendants
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)K1925503MTM AttestTM Super Rapid Steam Biological Indicator 1592, 3MTM AttestTM Super…3M Company2020—
+1K2138093M Attest Super Rapid Steam Biological Indicator, 3M Attest Super Rapid Steam…3M Company2022—
+2K2425383M™ Attest™ Super Rapid Readout Biological Indicator 1493; 3M™ Attest™ Super…3M Company2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199410
200210
201110
201810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202410
FIG. 1 — Lineage of K192550, 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
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
*K1734373M Attest Super Rapid Readout Biological Indicator 1492V, 3M Attest Auto-reader 490, 3M…
Summary page 6
…FRC] Predicate Device- Biological Indicator: 3M™ Attest™ Super Rapid Readout Biological Indicator 1492V, 3M™ Attest™ Auto-reader 490, and 3M™ Attest™ Auto-reader 490H, K173437 Indications for Use- Biological Indicator Use the 3M™ Attest™ Super Rapid Steam Biological Indicator 1592 in conjunction with t…
3M Company20181
*K1735193M Attest Super Rapid Readout Steam Challenge Pack, 3M Attest Super Rapid 5 Steam-Plus…
Summary page 11
…0(a), FRC] Predicate Device- Challenge Pack: 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- Challenge Pack Use the 3M™ Attest™ Super Rapid Steam Challenge Pack 51582 in conjunction with the 3M™ Atte…
3M Company20181

Also cleared against K173437: 2 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K2138093M Attest Super Rapid Steam Biological Indicator, 3M Attest Super Rapid Steam Challenge…3M Company20221

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 25 years and passes through 2 companies; a new generation was cleared every 3.5 years on median.
  • 3 of the 10 ancestors have a recall of any class.
  • Of its descendants, K213809 (3M Company, 2022) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K173437.

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 Steam Biological Indicator 1592 in conjunction with the 3M™ Attest™ Auto-reader 490 having software version 4.0.0 or greater or the 3M™ Attest™ Auto-reader 490H having software version 4.0.0 or greater to qualify or monitor the following sterilization cycles: Cycle Type Exposure Temperature Exposure Time Dynamic-air-removal (pre-vacuum and SFPP) 250°F (121°C) 15 minutes Dynamic-air-removal (pre-vacuum and SFPP) 250°F…

Read the full statement (144 words)

Use the 3M™ Attest™ Super Rapid Steam Biological Indicator 1592 in conjunction with the 3M™ Attest™ Auto-reader 490 having software version 4.0.0 or greater or the 3M™ Attest™ Auto-reader 490H having software version 4.0.0 or greater to qualify or monitor the following sterilization cycles:

Cycle Type Exposure Temperature Exposure Time

Dynamic-air-removal (pre-vacuum and SFPP) 250°F (121°C) 15 minutes

Dynamic-air-removal (pre-vacuum and SFPP) 250°F (121°C) 20 minutes

Dynamic-air-removal (pre-vacuum and SFPP) 250°F (121°C) 30 minutes

Dynamic-air-removal (pre-vacuum and SFPP) 250°F (121°C) 35 minutes

Gravity Displacement 250°F (121°C) 30 minutes

Use the 3M™ Attest™ Super Rapid Steam Challenge Pack 51582 in conjunction with the 3M™ Attest™ Auto-reader 490 having software version 4.0.0 or greater or the 3M™ Attest™ Auto-reader 490H having software version 4.0.0 or greater to qualify or monitor dynamic-air-removal (pre-vacuum and SFPP) or gravity displacement steam sterilization cycles of 30 minutes at 250°F (121°C).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192550: 3MTM AttestTM Super Rapid Steam Biological Indicator 1592, 3MTM AttestTM Super Rapid Steam Challenge Pack, 3MTM AttestTM Auto- Readers 490 and 490H.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192550

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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