MARQUETTE 1200 DEFIBRILLATION PADS— 510(k) K895651

Substantially Equivalent

Marquette Electronics, Inc.

FDA 510(k) clearance K895651 for MARQUETTE 1200 DEFIBRILLATION PADS, Substantially Equivalent on 1989-12-12. Applicant: Marquette Electronics, Inc..

Clearance details

Applicant: Marquette Electronics, Inc.
Product code: Code LDD
Advisory panel: Cardiovascular
Date received: 1989-09-20
Decision date: 1989-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: N. Ireland Bt19 2qy, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code LDD

product code LDD

Death: 38
Malfunction: 522
Total: 560

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.