510(k) · Cleared
ClearedAti Disposable Biological Test Pack for Steam Ster
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ati · FRC Indicator, Biological Sterilization Process
Cleared on Jul 19, 1990 after a 55-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 19 later devices descend from it.
- Decided
- Jul 19, 1990
- Review
- 55 days
- Class
- Class II
- Product code
- FRC
- Recalls
- None
- Predicates
- 0
19 later devices descend from it, 2 citing it directly.
- This deviceK902344 Ati Disposable Biological Test Pack for Steam SterAti · 1990
- Descendant · cites it directly · 12 of its ownK963841 EztestSgm Biotech, Inc. · 1997 · Recalled
- Descendant · cites it directly · 5 of its ownK930683 Eztest-GasSgm Biomedical, Inc. · 1997
- Descendant · 2 generations on · 3 of its ownK151585 Andersen EOGas 4 SteriTestAndersen Sterilizers, Inc. · 2015
- Descendant · 2 generations on · 3 of its ownK070595 Sporview Steam Self-Contained Biological IndicatorSpsmedical Supply Corp. · 2007
- Descendant · 3 generations on · 2 of its ownK111515 Spsmedical Sporview Steam BISpsmedical Supply Corp. · 2012
Showing 5 of 19 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 19 · See all- K963841EztestSgm Biotech, Inc. · 1997 · cites it directly12descendants
- K930683Eztest-GasSgm Biomedical, Inc. · 1997 · cites it directly5descendants
- K151585Andersen EOGas 4 SteriTestAndersen Sterilizers, Inc. · 2015 · 2 generations on3descendants
- K070595Sporview Steam Self-Contained Biological IndicatorSpsmedical Supply Corp. · 2007 · 2 generations on3descendants
- K111515Spsmedical Sporview Steam BISpsmedical Supply Corp. · 2012 · 3 generations on2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K902344 | Ati Disposable Biological Test Pack for Steam Ster | Ati | 1990 | — |
| +1 | K963841 | Eztest | Sgm Biotech, Inc. | 1997 | 1 |
| +1 | K930683 | Eztest-Gas | Sgm Biomedical, Inc. | 1997 | — |
| +2 | K151585 | Andersen EOGas 4 SteriTest | Andersen Sterilizers, Inc. | 2015 | — |
| +2 | K070595 | Sporview Steam Self-Contained Biological Indicator | Spsmedical Supply Corp. | 2007 | — |
| +3 | K111515 | Spsmedical Sporview Steam BI | Spsmedical Supply Corp. | 2012 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 2 | 0 |
| 2004 | 2 | 0 |
| 2007 | 2 | 0 |
| 2009 | 2 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2015 | 1 | 0 |
| 2017 | 2 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), 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 K250044 Celerity 5 HP Biological Indicator (LCB052)…score 14.5 · 10 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (19)
See all 192 later devices cite it directly; ranked here by how many devices descend from each in turn.
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?
- Of its descendants, K963841 (Sgm Biotech, Inc., 1997) has gone furthest, with 12 descendants of its own.
How does its category compare?
All FRC devicesFRC Indicator, Biological Sterilization Process: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FRC
6in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FRC
29in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FRC
8so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FRC
9in 2025
MAUDE reports naming product code FRC, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 3 | 83 | 0 | 100 |
| 2008 | 1 | — | 0 | 60 |
| 2009 | 6 | 183 | 1 | 45 |
| 2010 | 4 | 165 | 0 | 57 |
| 2011 | 6 | 118 | 0 | 37 |
| 2012 | 9 | 178 | 2 | 46 |
| 2013 | 4 | 260 | 2 | 39 |
| 2014 | 13 | 174 | 0 | 51 |
| 2015 | 3 | 130 | 0 | 182 |
| 2016 | 2 | — | 0 | 482 |
| 2017 | 10 | 130 | 0 | 182 |
| 2018 | 18 | 97 | 0 | 22 |
| 2019 | 5 | 88 | 0 | 30 |
| 2020 | 10 | 150 | 0 | 16 |
| 2021 | 5 | 107 | 0 | 10 |
| 2022 | 5 | 193 | 4 | 9 |
| 2023 | 6 | 190 | 1 | 20 |
| 2024 | 8 | 105 | 0 | 22 |
| 2025 | 6 | 29 | 0 | 9 |
| 2026 | 1 | — | 8 | — |
https://510kreport.com/device/K902344 · printed Nov 4, 2026
Cite this page
510(k) Report. “K902344: Ati Disposable Biological Test Pack for Steam Ster.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K902344
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026