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FDA 510(k)

A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX.

K-Number: K903691 · 1990-10-12

ApplicantTherex Corp.
Decision Date1990-10-12
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX. is the device name listed in this FDA 510(k) record. The listed applicant is Therex Corp.. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K903691. 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 IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX.?

A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX. is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Therex Corp.. The 510(k) number is K903691.

When did A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX. receive FDA 510(k) clearance?

A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX. received FDA 510(k) clearance on 1990-10-12, under 510(k) number K903691.

Who is the listed applicant for A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX.?

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 IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX.?

The FDA product code for A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX. 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.

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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