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FDA 510(k)

HMP DUAL TITANIUM PORT

K-Number: K934504 · 1994-02-25

ApplicantHorizon Medical Products, Inc.
Decision Date1994-02-25
Product CodeLJT
Advisory CommitteeHO
DecisionUnknown

Device Summary

HMP DUAL TITANIUM PORT is the device name listed in this FDA 510(k) record. The listed applicant is Horizon Medical Products, Inc.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K934504. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HMP DUAL TITANIUM PORT?

HMP DUAL TITANIUM PORT is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Horizon Medical Products, Inc.. The 510(k) number is K934504.

When did HMP DUAL TITANIUM PORT receive FDA 510(k) clearance?

HMP DUAL TITANIUM PORT received FDA 510(k) clearance on 1994-02-25, under 510(k) number K934504.

Who is the listed applicant for HMP DUAL TITANIUM PORT?

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

What is the FDA product code for HMP DUAL TITANIUM PORT?

The FDA product code for HMP DUAL TITANIUM PORT is LJT.

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Other records listing Horizon Medical Products, Inc. as applicant

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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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