MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM— 510(k) K873680

Substantially Equivalent

Oxford Medilog, Inc.

FDA 510(k) clearance K873680 for MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM, Substantially Equivalent on 1987-11-23. Applicant: Oxford Medilog, Inc..

Clearance details

Applicant: Oxford Medilog, Inc.
Product code: Code DSI
Advisory panel: Cardiovascular
Date received: 1987-09-14
Decision date: 1987-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

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Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

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.