HANSEN MEDICAL ARTISAN S CONTROL CATHETER— 510(k) K090365

Unknown

Hansen Medical, Inc.

FDA 510(k) clearance K090365 for HANSEN MEDICAL ARTISAN S CONTROL CATHETER, Unknown on 2009-05-07. Applicant: Hansen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Hansen Medical, Inc.
Product code: Code DXX
Device class: Class 2
Regulation: 21 CFR 870.1290
Advisory panel: Cardiovascular
Date received: 2009-02-13
Decision date: 2009-05-07
Decision: Unknown
Clearance type: Special
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.