K182503

Substantially Equivalent

Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors

Applicant: Physio-Control, Inc.
Product code: LDD
Advisory panel: Cardiovascular
Date received: 2018-09-12
Decision date: 2019-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, WA, US

Adverse events under product code LDD

product code LDD

Death: 38
Malfunction: 522
Total: 560

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.