510(k) Report

510(k) · Cleared

Cleared

Smart-Well Eztest Incubator

K091950510(k) TraditionalCleared Jan 15, 2010198-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

Sgm Biotech, Inc. · FRC Indicator, Biological Sterilization Process

Cleared on Jan 15, 2010 as substantially equivalent to K855101 (Surgicot, Inc., 1986) after a 198-day review. Its family tree reaches back 1 generation to 1986.

Decided
Jan 15, 2010
Review
198 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K855101 (1986). No later device cites it as a predicate yet.

K855101 · Assert TM Biological/Chemical Indicator · Surgicot, Inc. · 1986198519901995200020052010
  1. Root · 1 generation backK855101 Assert TM Biological/Chemical IndicatorSurgicot, Inc. · 1986
  2. This deviceK091950 Smart-Well Eztest IncubatorSgm Biotech, Inc. · 2010
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K855101Assert TM Biological/Chemical IndicatorSurgicot, Inc.1986—
0 (this device)K091950Smart-Well Eztest IncubatorSgm Biotech, Inc.2010—
FIG. 1 — Lineage of K091950, 1986–2010Source: 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
*K855101Assert TM Biological/Chemical Indicator
Summary page 1
…) Product Code: Accessory to FRC Predicate Device: Sterise Verifym Incubator submitted with the Steris Verify' SCBI. Predicate Device 510kNumber: K855 101 Performance Standards: The Smart-Read EZTest SCBI for monitoring steam sterilization processes complies to the following FDA rec…
Surgicot, Inc.1986—

Also cleared against K855101: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • Its one ancestor has no recall.
  • 2 other devices also cite its predicate K855101.

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. 2010, 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 Smart-Well incubator is intended for use with the Smart-Read EZTest self-contained biological indicators (SCBI1). The Smart-Read EZTest - steam SCBI3 is used for monitoring the efficacy of gravity or pre-vac saturated steam sterilizati on processes. This SGBI1 contains I05 spores of Geobacillus stearothennophilus derived from ATCC #7953. Performance characteristics were established in accordance with USP 32 and ISO 11138-1 for the 1210 C steam…

Read the full statement (642 words)

The Smart-Well incubator is intended for use with the Smart-Read EZTest self-contained biological indicators (SCBI1). The Smart-Read EZTest - steam SCBI3 is used for monitoring the efficacy of gravity or pre-vac saturated steam sterilizati on processes. This SGBI1 contains I05 spores of Geobacillus stearothennophilus derived from ATCC #7953. Performance characteristics were established in accordance with USP 32 and ISO 11138-1 for the 1210 C steam process. Additional saturated steam sterilization conditions are also tested and appear on the Certificate of Analysis for Smart-Read EZest - steam. These include 132 0 C, l34'C, and 135'CC

The operational principles of the device are as follows. The Smart-Read EZest - steam SCHI3 is placed into a difficult to sterilize position in the load and a sterilization cycle appropriate for the particular type~of load is run. As sterilization conditions are met, the bacterial spores are destroyed by logarithmic thermal death principles. Following the sterilization cycle, the operator removes the SCBI from the load and waits approximately 10 minutes until the device has cooled so it can be comfortably handled. The'operator then places the'SCBI3 in the activation cavity of the Smart-Well incubator. The SCBI is then gently tilted forward towards the operator to fracture the glass media ampoule inside the plastic sleeve. This allows the culture media to mix with any surviving spores in the SCB3I. The activated BI is then placed into one of the ten incubator cavities. The Smart-Well incubator provides a constant pie-set temperature of 60-f- 2 0 C which is conducive to growth of any bacterial spores which may have survived the sterilization process. The unit is also supplied with an NIST traceable thermomneter to independently indicate the incubator block temperature. Growth of the indicator organisms will produce acid in the microbiological culture mediumecontaining bromcresol purple, thus lowejing the pH-of the solution and invoking a yellow color change of the media components. If all spores have been killed, the media will remain clear and purple. The-mediamneets the requirements for growth promotion.

When the activated SCBI is placed into one of the incubation cavities the LED in front of the cavity will illuminate amber, which indicates that the incubator electronically recognizes the Smart-Read EZTest SCBI unit for incubation. Each incubation cavity also has an electronic monitoring system that detects if the BKis either purple or yellow.

The Smart-Well incubator can also be supplied with a printer whichidocuments each individual EZTest steam SCBI tested. The printer can also display information that is normally manually entered into a log book. The recommended incubation hold time of IO hours has been established using the FDA CDRH Reduced Incubation Time protocol. The printer can also be configured to display HI exposure information that includes 1) exposure time and temperature; 2) cycle type; 3) sterilizer number; 4) HI lot number; and 5) user identification. These are optional entries. If no selection is made, the printed report will default to the previously entered information of place a "?" mark or blank indicating no selection was made

The printed record will always indicate real time and date, incubation cavity being reported, the incubation start time when the SCBI was placed into the incubation cavity, and the time the test status changed. The result options art 1) NEGATIVE (purple) - incubation time completed with no detectable color change in the Smart-Read EZTest unit, 2) POSITIVE (yellow) - time that a yellow color was detected in the Smart-Read EZTest unit, or 3) TESTING - when a printout is requested and event 1) or 2) have not happened. These results are easily verified by the user as performed in all conventional incubators without printers.

The incubated SCOBI should be properly disposed of after the results have been properly recorded. The recommended disposal is to "sterilize by steam 12100C for not less then 30 minutes" of follow your institution's practice for disposal or biological waste.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K091950: Smart-Well Eztest Incubator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K091950

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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