FDA 510(k)

TARGET VITAL-PORT VASCULAR ACCESS SYSTEM

K-Number: K970442 · 1997-04-30

Decision Date1997-04-30

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

TARGET VITAL-PORT VASCULAR ACCESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Med Institute, Inc.. It received FDA 510(k) clearance on 1997-04-30 under 510(k) number K970442. 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 TARGET VITAL-PORT VASCULAR ACCESS SYSTEM?

TARGET VITAL-PORT VASCULAR ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 1997-04-30. The listed applicant is Med Institute, Inc.. The 510(k) number is K970442.

When did TARGET VITAL-PORT VASCULAR ACCESS SYSTEM receive FDA 510(k) clearance?

TARGET VITAL-PORT VASCULAR ACCESS SYSTEM received FDA 510(k) clearance on 1997-04-30, under 510(k) number K970442.

Who is the listed applicant for TARGET VITAL-PORT VASCULAR ACCESS SYSTEM?

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

What is the FDA product code for TARGET VITAL-PORT VASCULAR ACCESS SYSTEM?

The FDA product code for TARGET VITAL-PORT VASCULAR ACCESS SYSTEM 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 Med Institute, Inc. as applicant

K990034WILSON-COOK COLONIC Z-STENT K982507MINI POLYURETHANE CATHETER K981061INTRAVASCULAR RETRIEVAL DEVICE K964001SWARTZ DOPPLER FLOW PROBE AND MONITOR SYSTEM K971140VITAL-PORT INFUSION PAL K945586FLEXIBLE DILATING SHEATH

View all 26 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.