CORDIS PERVENOUS ATRIAL LEAD— 510(k) K810432

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K810432 for CORDIS PERVENOUS ATRIAL LEAD, Substantially Equivalent on 1981-03-13. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code DTB
Advisory panel: Cardiovascular
Date received: 1981-02-19
Decision date: 1981-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DTB

product code DTB

Death: 1,491
Injury: 67,311
Malfunction: 79,368
Other: 10
Total: 148,180

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.