S&W ELECTRODE TYPES 888, 844, 988 AND 944— 510(k) K864586

Substantially Equivalent

S & W Medico Teknik

FDA 510(k) clearance K864586 for S&W ELECTRODE TYPES 888, 844, 988 AND 944, Substantially Equivalent on 1987-03-13. Applicant: S & W Medico Teknik.

Clearance details

Applicant: S & W Medico Teknik
Product code: Code DRX
Advisory panel: Cardiovascular
Date received: 1986-11-21
Decision date: 1987-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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Adverse events under product code DRX

product code DRX

Death: 6
Injury: 476
Other: 2
Total: 484

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.