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FDA 510(k)

A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT

K-Number: K896093 · 1989-12-06

ApplicantTherex Corp.
Decision Date1989-12-06
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT is the device name listed in this FDA 510(k) record. The listed applicant is Therex Corp.. It received FDA 510(k) clearance on 1989-12-06 under 510(k) number K896093. 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 A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT?

A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT is a medical device that received FDA 510(k) clearance on 1989-12-06. The listed applicant is Therex Corp.. The 510(k) number is K896093.

When did A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT receive FDA 510(k) clearance?

A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT received FDA 510(k) clearance on 1989-12-06, under 510(k) number K896093.

Who is the listed applicant for A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT?

The FDA 510(k) record lists Therex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT?

The FDA product code for A-PORT IMPLANT. VASCULAR ACCESS SYSTEM - A2PORT is LJT.

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Other records listing Therex Corp. 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.

K953110LOW PROFILE TITANIUM MODEL CATALOG #1003K953017LOW PROFILE TITANIUM MODEL CATALOG #1003K952537THEREX LOW PROFILE TITANIUM MODEL 1.0MM I.D./1.8MM O.D.K950212A2 DETACHED DUAL PORT SYSTEMK9501311.0MM 1.8MMO.D. POLYURETHANE DETACHED MODELK942412THEREX LOW-PROFILE PORT - TITANIUM MODEL

View all 26 devices →

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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