510(k) Report

510(k) · Cleared

Cleared

Alcon Multi-Purpose Disinfecting Solution ID 90746

K974624510(k) TraditionalCleared Mar 4, 199883-day reviewClass II21 CFR 886.5928

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

Alcon Laboratories · LPN Accessories, Soft Lens Products

Cleared on Mar 4, 1998 after an 83-day review; its predicate, P830034, is listed below. 1 later device descends from it.

Decided
Mar 4, 1998
Review
83 days
Class
Class II
Product code
LPN
Recalls
None
Predicates
1

1 ancestor in all. 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared1995200020052010201520202025
  1. This deviceK974624 Alcon Multi-Purpose Disinfecting Solution ID 90746Alcon Laboratories · 1998
  2. Descendant · cites it directly · 0 of its ownK021143 Opti-Free Express Multi-Purpose Disinfecting SolutionAlcon Universal, Ltd. · 2002 · Recalled

Most influential descendants

Showing 1 of 1 · See all
  • K021143Opti-Free Express Multi-Purpose Disinfecting SolutionAlcon Universal, Ltd. · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K974624Alcon Multi-Purpose Disinfecting Solution ID 90746Alcon Laboratories1998—
+1K021143Opti-Free Express Multi-Purpose Disinfecting SolutionAlcon Universal, Ltd.20021

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K974624, 1998–2002Source: 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 LPN? 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 LPN device

  1. #1 K253795 MeniSept 3% Hydrogen Peroxide Cleaning &…score 12.7 · 4 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
*P830034Polyquat Disinfection System
FDA lists this PMA only through its supplements; the earliest we hold is P830034/S001 (Oct 22, 1985).
Summary page 1
…e, to OPTI-FREE® EXPRESS Multi-Purpose Solution, OPTI-ONE® \'.’ Multi-Purpose Solution and OPTI-FREE® Rinsing, Disinfecting and Storage Solution, all approved under PMA 830034. Alcon Multi-Purpose Disinfecting Solution ID 90746 meets the 444 guidelines set forth in FDA’s May 1, 1997 Guid…
Alcon Laboratories—

Also cleared against P830034: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K021143Opti-Free Express Multi-Purpose Disinfecting SolutionAlcon Universal, Ltd.20020

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, K021143 (Alcon Universal, Ltd., 2002) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate P830034.

How does its category compare?

All LPN devices

LPN Accessories, Soft Lens Products: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LPN

2in 2022

2007: 42009: 12010: 22011: 32012: 22013: 22015: 22016: 32017: 12019: 22020: 32021: 22022: 22026 (partial year): 1
2007high 4 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LPN

167in 2020

2007: 175 days median2011: 222 days median2016: 59 days median2020: 167 days median
2007high 222 (2011) · low 59 (2016)2026

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

Recalls per year · LPN

1in 2020

2007: 22009: 22010: 22011: 12016: 12020: 1
2007high 2 (2007) · low 0 (2008)2026

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

Adverse event reports per year · LPN

40in 2025

2007: 1,1512008: 1532009: 1212010: 2412011: 2732012: 2682013: 842014: 1052015: 1762016: 4982017: 2,6662018: 952019: 602020: 822021: 512022: 622023: 842024: 762025: 40
2007high 2,666 (2017) · low 40 (2025)2025

MAUDE reports naming product code LPN, 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
2007417521,151
20080—0153
20091—2121
20102—2241
201132221273
20122—0268
20132—084
20140—0105
20152—0176
20163591498
20171—02,666
20180—095
20192—060
20203167182
20212—051
20222—062
20230—084
20240—076
20250—040
20261—0—

What is it indicated for?

For the daily cleaning, rinsing, disinfecting, and storing of soft (hydrophilic) contact lenses as recommended by your eye care practitioner. For use in chemical (not heat) disinfection.

Alcon Multi-Purpose Disinfecting Solution ID 90746 can also be used as a diluent for OPTI-FREE® SUPRACLENS® Daily Protein Remover.

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. “K974624: Alcon Multi-Purpose Disinfecting Solution ID 90746.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K974624

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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