REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406— 510(k) K024243

Substantially Equivalent

Fox Hollow Technologies

FDA 510(k) clearance K024243 for REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406, Substantially Equivalent on 2003-06-20. Applicant: Fox Hollow Technologies.

Clearance details

Applicant: Fox Hollow Technologies
Product code: Code MCW
Advisory panel: Cardiovascular
Date received: 2002-12-23
Decision date: 2003-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redwood City, CA, US

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Adverse events under product code MCW

product code MCW

Death: 38
Injury: 1,386
Malfunction: 2,676
Other: 2
Total: 4,102

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.