CARDIO-SCOPE MINI MONITOR— 510(k) K831878

Substantially Equivalent

W.E. Leder Enterprises, Inc.

FDA 510(k) clearance K831878 for CARDIO-SCOPE MINI MONITOR, Substantially Equivalent on 1983-09-29. Applicant: W.E. Leder Enterprises, Inc..

Clearance details

Applicant: W.E. Leder Enterprises, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1983-06-13
Decision date: 1983-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.