510(k) Report

510(k) · Cleared

Cleared

Sporicidin Sterilizing and Disinfecting Solution (SSDS)

K983194510(k) TraditionalCleared Mar 5, 1999175-day reviewClass II21 CFR 880.6885

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Sporicidin Intl. · MED Sterilant, Medical Devices

Cleared on Mar 5, 1999 after a 175-day review. The FDA summary names its predicate without a number.

Decided
Mar 5, 1999
Review
175 days
Class
Class II
Product code
MED
Recalls
None
Predicates
0

The FDA summary names its predicate without a number.

FIG. 1 — Lineage of K983194Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

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 MED? 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 MED device

  1. #1 K251666 SYSTEM 1E Liquid Chemical Sterilant Processing…score 13.8 · 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? (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
*—CIDEX® Activated Dialdehyde Solution
Named without a submission number
—

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.

How does its category compare?

All MED devices

MED Sterilant, Medical Devices: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MED

2in 2023

2007: 22008: 12010: 62012: 32013: 12014: 12016: 12017: 12018: 22019: 42021: 22022: 12023: 22026 (partial year): 2
2007high 6 (2010) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MED

84in 2019

2010: 281 days median2012: 111 days median2019: 84 days median
2007high 281 (2010) · low 84 (2019)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MED

2in 2011

2007: 32008: 22011: 2
2007high 3 (2007) · low 0 (2009)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MED

9in 2025

2007: 342008: 792009: 1582010: 892011: 1062012: 3372013: 1402014: 1052015: 1102016: 1352017: 742018: 422019: 352020: 322021: 312022: 162023: 92024: 82025: 9
2007high 337 (2012) · low 8 (2024)2025

MAUDE reports naming product code MED, 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
20072—334
20081—279
20090—0158
20106281089
20110—2106
201231110337
20131—0140
20141—0105
20150—0110
20161—0135
20171—074
20182—042
2019484035
20200—032
20212—031
20221—016
20232—09
20240—08
20250—09
20262—0—

What is it indicated for?

Sporicidin® Sterilizing and Disinfecting Solution (SSDS) is intended for sterilization or high level disinfection of medical and surgical instruments that require submersion. SSDS is intended for reprocessing only heat-sensitive medical devices. Sporicidin® Sterilizing and Disinfecting Solution (SSDS) should be used under the following contact conditions: Sterilization: 12 hours at 25 degrees C High Level Disinfection: 20 minutes at 25 degrees C SSDS can…

Read the full statement (129 words)

Sporicidin® Sterilizing and Disinfecting Solution (SSDS) is intended for sterilization or high level disinfection of medical and surgical instruments that require submersion. SSDS is intended for reprocessing only heat-sensitive medical devices.

Sporicidin® Sterilizing and Disinfecting Solution (SSDS) should be used under the following contact conditions:

Sterilization: 12 hours at 25 degrees C

High Level Disinfection: 20 minutes at 25 degrees C

SSDS can be reused for a maximum of 7 days or until Sporicidin Test Strips indicate that either the glutaraldehyde or phenol level falls below its Minimum Recommended Concentration (MRC). The glutaraldehyde MRC is 0.6%; the phenol MRC is 1.3%.

Sporicidin Indicator Strips are intended for verifying the MRC of glutaraldehyde and phenol in SSDS during use. Sporicidin Indicator strips should be used before each use of SSDS.

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. “K983194: Sporicidin Sterilizing and Disinfecting Solution (SSDS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K983194

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026