510(k) Report

510(k) · Cleared

Recalled · Class II · 2024

Sporview

K905425510(k) TraditionalCleared Mar 27, 1992479-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

Spsmedical Supply Corp. · FRC Indicator, Biological Sterilization Process

Cleared on Mar 27, 1992 after a 479-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it. It has been recalled 2 times.

Decided
Mar 27, 1992
Review
479 days
Class
Class II
Product code
FRC
Recalls
2
Predicates
0

4 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared1997: 1 descendant cleared1996: 1 descendant cleared2004: 1 descendant cleared1990200020102020
  1. This deviceK905425 SporviewSpsmedical Supply Corp. · 1992
  2. Descendant · cites it directly · 1 of its ownK023716 Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp. · 2002 · Recalled
  3. Descendant · cites it directly · 0 of its ownK041099 Modification to Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp. · 2004 · Recalled
  4. Descendant · cites it directly · 0 of its ownK971432 ProsporeRaven Biological Laboratories, Inc. · 1997 · Recalled
  5. Descendant · cites it directly · 0 of its ownK962441 Prospore (Stearo for Steam Sterilizer)Raven Biological Laboratories, Inc. · 1996

Most influential descendants

Showing 4 of 4 · See all
  • K023716Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp. · 2002 · cites it directly1descendant
  • K041099Modification to Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp. · 2004 · cites it directly0descendants
  • K971432ProsporeRaven Biological Laboratories, Inc. · 1997 · cites it directly0descendants
  • K962441Prospore (Stearo for Steam Sterilizer)Raven Biological Laboratories, Inc. · 1996 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K905425SporviewSpsmedical Supply Corp.1992—
+1K023716Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp.20021
+1K041099Modification to Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp.20041
+1K971432ProsporeRaven Biological Laboratories, Inc.19973
+1K962441Prospore (Stearo for Steam Sterilizer)Raven Biological Laboratories, Inc.1996—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
200210
200410
FIG. 1 — Lineage of K905425, 1992–2004Source: 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), 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
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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? (4)

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

NumberDeviceApplicantDecidedDescendants
K023716Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp.20021
K041099Modification to Spsmedical Sporview Bacterial Spore StripSpsmedical Supply Corp.20040
K971432ProsporeRaven Biological Laboratories, Inc.19970
K962441Prospore (Stearo for Steam Sterilizer)Raven Biological Laboratories, Inc.19960

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

Recalls of this device

DateClassRecallRoot causeReason
Dec 11, 2024Class IIZ-1141-2025Error in labelingSpore test strip monitoring system, designed for routine monitoring of sterilization processes, may have a printing error on the return envelope that may cause spore test results to be reported to the incorrect customer's account.
May 25, 2022Class IIIZ-1790-2022Environmental controlFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K023716 (Spsmedical Supply Corp., 2002) has gone furthest, with 1 descendant of its own.

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—
Cite this page

510(k) Report. “K905425: Sporview.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K905425

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026