RAPID INTRAVASCULAR CATHETER START SYSTEM 22 GAUGE / 20 GAUGE / 18 GAUGE— 510(k) K112347

Substantially Equivalent

Vascular Pathways, Inc.

FDA 510(k) clearance K112347 for RAPID INTRAVASCULAR CATHETER START SYSTEM 22 GAUGE / 20 GAUGE / 18 GAUGE, Substantially Equivalent on 2011-09-22. Applicant: Vascular Pathways, Inc..

Clearance details

Applicant: Vascular Pathways, Inc.
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 2011-08-15
Decision date: 2011-09-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Orinda, CA, US

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Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.