K890988

Substantially Equivalent

MODEL 3110 HEART WIRE & 3110P PEDIATRIC HEART WIRE

Applicant: Pace Medical
Product code: LDF
Advisory panel: Cardiovascular
Date received: 1989-02-27
Decision date: 1989-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

Adverse events under product code LDF

product code LDF

Death: 19
Injury: 188
Malfunction: 694
Other: 1
Total: 902

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.