K924434

Substantially Equivalent

CIDEX ACTIVATED DIALDEHYDE SOLUTION

Applicant: Johnson & Johnson Medical, Inc.
Product 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

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.