Comet Pressure Guidewire— 510(k) K151610

Substantially Equivalent

Boston Scientific Corporation

FDA 510(k) clearance K151610 for Comet Pressure Guidewire, Substantially Equivalent on 2015-10-06. Applicant: Boston Scientific Corporation.

Clearance details

Applicant: Boston Scientific Corporation
Product code: Code DXO
Advisory panel: Cardiovascular
Date received: 2015-06-15
Decision date: 2015-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fremont, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXO

product code DXO

Death: 10
Injury: 156
Malfunction: 884
Total: 1,050

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.