510(k) Report

510(k) · Cleared

Cleared

Prospore (Stearo for Steam Sterilizer)

K962441510(k) TraditionalCleared Sep 18, 199686-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

Raven Biological Laboratories, Inc. · FRC Indicator, Biological Sterilization Process

Cleared on Sep 18, 1996 as substantially equivalent to K905425 (Spsmedical Supply Corp., 1992) after an 86-day review. Its family tree reaches back 1 generation to 1992.

Decided
Sep 18, 1996
Review
86 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K905425 (1992). No later device cites it as a predicate yet.

K905425 · Sporview · Spsmedical Supply Corp. · 1992 · recalled19901992199419961998
K905425 · Sporview · Spsmedical Supply Corp. · 1992 · recalled0
  1. Root · 1 generation backK905425 SporviewSpsmedical Supply Corp. · 1992 · Recalled
  2. This deviceK962441 Prospore (Stearo for Steam Sterilizer)Raven Biological Laboratories, Inc. · 1996
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K905425SporviewSpsmedical Supply Corp.19922
0 (this device)K962441Prospore (Stearo for Steam Sterilizer)Raven Biological Laboratories, Inc.1996—
FIG. 1 — Lineage of K962441, 1992–1996Source: 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

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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
*K905425Sporview
Summary page 1
…Hospital Predicate Devices (legally marketed) Kilt™ (BBL) SporView™ (SPSmedical) Predicate Devices S10(k) number: Kilit™(BBL) - Grandfather In* SporView™ (SPSmedical) K905425 Description ProSpore® is aself-contained biological indicator used for determining the efficiency of a 121°C steam sterilizatio…
Spsmedical Supply Corp.19922
*—Kilt™ (BBL)
Named without a submission number
—

Also cleared against K905425: 3 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 a recall.
  • 3 other devices also cite its predicate K905425.

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.

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?

ProSpore® is a self-contained biological indicator used for determining the efficiency of a 121°C steam sterilization cycle.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K962441: Prospore (Stearo for Steam Sterilizer).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K962441

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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