510(k) K011373— INSTRUMENT DAMPING PORT

Substantially Equivalent

Medcanica, Inc.

Clearance details

Applicant: Medcanica, Inc.
Product code: Code DRC
Advisory panel: Cardiovascular
Date received: 2001-05-04
Decision date: 2001-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Adverse events under product code DRC

product code DRC

Death: 28
Injury: 412
Total: 440

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.