MICROVASIVE PULMONARY GUIDEWIRE— 510(k) K022059

Substantially Equivalent

Boston Scientific Corp

FDA 510(k) clearance K022059 for MICROVASIVE PULMONARY GUIDEWIRE, Substantially Equivalent on 2002-11-13. Applicant: Boston Scientific Corp.

Clearance details

Applicant: Boston Scientific Corp
Product code: Code MDM
Advisory panel: General, Plastic Surgery
Date received: 2002-06-25
Decision date: 2002-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Natick,, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MDM

product code MDM

Injury: 247
Malfunction: 1,516
Total: 1,763

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.