PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA— 510(k) K834358
Substantially EquivalentVas-Cath of Canada , Ltd.
FDA 510(k) clearance K834358 for PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA, Substantially Equivalent on 1984-04-02. Applicant: Vas-Cath of Canada , Ltd..
Clearance details
- Applicant
- Vas-Cath of Canada , Ltd.
- Product code
- Code FIQ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.