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FDA 510(k)

VITAL-PORT VASCULAR ACCESS SYSTEM

K-Number: K934520 · 1994-09-06

ApplicantMed Institute, Inc.
Decision Date1994-09-06
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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 1994-09-06 under 510(k) number K934520. 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 VITAL-PORT VASCULAR ACCESS SYSTEM?

VITAL-PORT VASCULAR ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 1994-09-06. The listed applicant is Med Institute, Inc.. The 510(k) number is K934520.

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

VITAL-PORT VASCULAR ACCESS SYSTEM received FDA 510(k) clearance on 1994-09-06, under 510(k) number K934520.

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

The FDA product code for VITAL-PORT VASCULAR ACCESS SYSTEM is LJT.

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Other records listing Med Institute, Inc. as applicant

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.

K990034WILSON-COOK COLONIC Z-STENTK982507MINI POLYURETHANE CATHETERK981061INTRAVASCULAR RETRIEVAL DEVICEK964001SWARTZ DOPPLER FLOW PROBE AND MONITOR SYSTEMK971140VITAL-PORT INFUSION PALK970442TARGET VITAL-PORT VASCULAR ACCESS SYSTEM

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Related Devices (Code: LJT)

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.

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.

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