pNOVUS 21 Microcatheter— 510(k) K221279

Substantially Equivalent

Phenox, Ltd.

FDA 510(k) clearance K221279 for pNOVUS 21 Microcatheter, Substantially Equivalent on 2022-11-28. Applicant: Phenox, Ltd..

Clearance details

Applicant: Phenox, Ltd.
Product code: Code DQO
Advisory panel: Cardiovascular
Date received: 2022-05-03
Decision date: 2022-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galway, IE

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQO

product code DQO

Death: 35
Injury: 993
Malfunction: 1,772
Other: 5
Total: 2,805

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.