CONMED ECG PATIENT CABLES AND LEADWIRES— 510(k) K933649

Substantially Equivalent

Conmedcorp

FDA 510(k) clearance K933649 for CONMED ECG PATIENT CABLES AND LEADWIRES, Substantially Equivalent on 1994-02-18. Applicant: Conmedcorp.

Clearance details

Applicant: Conmedcorp
Product code: Code DSA
Advisory panel: Cardiovascular
Date received: 1993-07-27
Decision date: 1994-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Utica, NY, US

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Adverse events under product code DSA

product code DSA

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.