PIOLAX HYDROPHILIC GUIDEWIRE— 510(k) K980977

Substantially Equivalent

Piolax Medical Devices, Inc.

FDA 510(k) clearance K980977 for PIOLAX HYDROPHILIC GUIDEWIRE, Substantially Equivalent on 1998-10-27. Applicant: Piolax Medical Devices, Inc..

Clearance details

Applicant: Piolax Medical Devices, Inc.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 1998-03-16
Decision date: 1998-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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.