HYDRAVIEW GUIDEWIRE— 510(k) K141831

Substantially Equivalent

Brivant Limited

FDA 510(k) clearance K141831 for HYDRAVIEW GUIDEWIRE, Substantially Equivalent on 2014-09-04. Applicant: Brivant Limited.

Clearance details

Applicant: Brivant Limited
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 2014-07-07
Decision date: 2014-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galway, IE

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQX

product code DQX

Death: 298
Injury: 4,385
Malfunction: 7,203
Other: 5
Total: 11,891

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.