ELECTRODE SERIES 1600— 510(k) K760358

Substantially Equivalent

Andover Medical, Inc.

FDA 510(k) clearance K760358 for ELECTRODE SERIES 1600, Substantially Equivalent on 1976-08-23. Applicant: Andover Medical, Inc..

Clearance details

Applicant: Andover Medical, Inc.
Product code: Code DRX
Advisory panel: Cardiovascular
Date received: 1976-08-02
Decision date: 1976-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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.