FDA 510(k)

NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS

K-Number: K112713 · 2011-10-27

Decision Date2011-10-27

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Medical Products, Inc.. It received FDA 510(k) clearance on 2011-10-27 under 510(k) number K112713. 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 NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS?

NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS is a medical device that received FDA 510(k) clearance on 2011-10-27. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K112713.

When did NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS receive FDA 510(k) clearance?

NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS received FDA 510(k) clearance on 2011-10-27, under 510(k) number K112713.

Who is the listed applicant for NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS?

The FDA 510(k) record lists Norfolk Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS?

The FDA product code for NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTS is LJT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Norfolk Medical Products, Inc. as applicant

K192291TidalPort-AP Implantable Apheresis Vascular Access Port K102385NORFOLK MEDICAL NORPORT FAMILY OF PORTS K942784NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED K896544MD2 PERSONAL INFUSION SYSTEM K872838NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)K871209NORFOLK MEDICAL NORPORT

View all 20 devices →

Related Devices (Code: LJT)

K260916FLEXI-PORT™ Power Injectable Implantable PortPortal Access, Inc.K252478Vaccess™ CT Low-Profile Power-Injectable Implantable Port; Vaccess™ CT Power-Injectable Implantable Port; PowerPort™ duo M.R.I. ™ Implantable PortBard Access Systems, Inc.K251253PowerPort™ isp Implantable Port; PowerPort™ Slim Implantable Port; PowerPort™ M.R.I. ™ Implantable Port; PowerPort™ M.R.I.™ isp Implantable PortBard Access Systems, Inc.K242328PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim Implantable PortsBard Access Systems, 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.K190559SmartPort+ Implantable Ports, SmartPort Plastic Implantable PortsAngioDynamics, 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.