K885240

Substantially Equivalent

MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD

Applicant: Tpl-Cordis, Inc.
Product code: DTB
Advisory panel: Cardiovascular
Date received: 1988-12-21
Decision date: 1989-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

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.