Home » AngioDynamics Earns 510(k) Clearance and CE Mark for Implantable Port
AngioDynamics Earns 510(k) Clearance and CE Mark for Implantable Port
New York-based AngioDynamics said it has received 510(k) clearance from the FDA and a CE mark in Europe for its SmartPort+ implantable port.
The subcutaneous port provides long-term access for blood specimen withdrawal and the administration of fluids to patients.
The company said it will immediately launch the product in the U.S. and Europe.
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