CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM
K-Number: K880571 · 1988-03-04
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Device Summary
Frequently Asked Questions
What is the CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM?
CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Catheter Technology Corp.. The 510(k) number is K880571.
When did CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM receive FDA 510(k) clearance?
CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM received FDA 510(k) clearance on 1988-03-04, under 510(k) number K880571.
Who is the listed applicant for CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM?
The FDA 510(k) record lists Catheter Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM?
The FDA product code for CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM 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 Catheter Technology 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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