ECG MONITOR MODEL RM102— 510(k) K851496

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K851496 for ECG MONITOR MODEL RM102, Substantially Equivalent on 1985-07-24. Applicant: Honeywell, Inc..

Clearance details

Applicant: Honeywell, Inc.
Product code: Code DXJ
Advisory panel: Cardiovascular
Date received: 1985-04-15
Decision date: 1985-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantville, NY, US

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Adverse events under product code DXJ

product code DXJ

Death: 2
Total: 2

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.