CIDEX ACTIVATED DIALDEHYDE SOLUTION— 510(k) K924434

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..

Clearance details

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

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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.