MULTICOR GAMMA 402 SERIES PACER— 510(k) K851419

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K851419 for MULTICOR GAMMA 402 SERIES PACER, Substantially Equivalent on 1985-06-11. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code DXY
Advisory panel: Cardiovascular
Date received: 1985-04-09
Decision date: 1985-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXY

product code DXY

Death: 240
Injury: 2,328
Malfunction: 2,096
Total: 4,664

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.