A-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EX.
K-Number: K903691 · 1990-10-12
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Device Summary
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.
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
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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