CIDEX ACTIVATED DIALDEHYDE SOLUTION— 510(k) K924434

Name: FDA 510(k) clearance K924434
Creator: U.S. Food and Drug Administration
Published: 1994-03-29

Substantially Equivalent

Johnson & Johnson Medical, Inc.

FDA 510(k) clearance K924434 for CIDEX ACTIVATED DIALDEHYDE SOLUTION, Substantially Equivalent on 1994-03-29. Applicant: Johnson & Johnson Medical, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Medical, Inc.
Product code: Code LRJ
Device class: Class 1
Regulation: 21 CFR 880.6890
Advisory panel: General Hospital
Date received: 1992-09-01
Decision date: 1994-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LRJ

product code LRJ

Injury: 958
Total: 958

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.