NMI DUAL PORT II
K-Number: K151239 · 2016-06-06
ApplicantNavilyst Medical, Inc.
Decision Date2016-06-06
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
NMI DUAL PORT II is a medical device manufactured by Navilyst Medical, Inc.. It received FDA 510(k) clearance on 2016-06-06 under approval number K151239. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NMI DUAL PORT II?
NMI DUAL PORT II is a medical device that received FDA 510(k) clearance on 2016-06-06. It is manufactured by Navilyst Medical, Inc.. The 510(k) number is K151239.
When was NMI DUAL PORT II approved by the FDA?
NMI DUAL PORT II received FDA 510(k) clearance on 2016-06-06, under approval number K151239.
What company makes NMI DUAL PORT II?
NMI DUAL PORT II is manufactured by Navilyst Medical, Inc..
What is the FDA product code for NMI DUAL PORT II?
The FDA product code for NMI DUAL PORT II is LJT.
Other Devices by Navilyst Medical, Inc.
Related Devices (Code: LJT)
K153359BardPort®, SlimPort®, and X-Port® Implanted PortsC.R. Bard, Inc.
K153238Dignity Dual PortMedcomp ( Medical Components)
K181446Bard Power-Injectable Implantable Ports (PowerPorts®)C.R. Bard, Inc.
K190559SmartPort+ Implantable Ports, SmartPort Plastic Implantable PortsAngioDynamics, Inc.
K232737PowerPort ClearVUE Slim ECG Enabled Implantable Port; PowerPort ClearVUE isp ECG Enabled Implantable Port; PowerPort isp M.R.I. ECG Enabled Implantable Port; PowerPort Slim ECG Enabled Implantable PortBard Peripheral Vascular, Inc.
K242328PowerPort ClearVUE Slim Implantable Ports and PowerPort ClearVUE Slim Implantable PortsBard Access Systems, Inc.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.