PORTABLE DEFIBRILLATOR MONITOR 74DRK— 510(k) K831696

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K831696 for PORTABLE DEFIBRILLATOR MONITOR 74DRK, Substantially Equivalent on 1983-11-03. Applicant: Honeywell, Inc..

Clearance details

Applicant: Honeywell, Inc.
Product code: Code LDD
Advisory panel: Cardiovascular
Date received: 1983-05-25
Decision date: 1983-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code LDD

product code LDD

Death: 38
Malfunction: 522
Total: 560

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.