Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter— 510(k) K151638

Substantially Equivalent

Cathera, Inc.

FDA 510(k) clearance K151638 for Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter, Substantially Equivalent on 2015-11-13. Applicant: Cathera, Inc..

Clearance details

Applicant: Cathera, Inc.
Product code: Code DQY
Advisory panel: Cardiovascular
Date received: 2015-06-17
Decision date: 2015-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQY

product code DQY

Death: 464
Injury: 4,489
Malfunction: 13,721
Other: 2
Total: 18,676

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.