K954719

Substantially Equivalent - Subject to Tracking Reg.

INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD

Applicant: Intermedics, Inc.
Product code: DTB
Advisory panel: Cardiovascular
Date received: 1995-10-13
Decision date: 1996-02-27
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Traditional
Location: Angleton, TX, 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.