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FDA 510(k)

CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM

K-Number: K880571 · 1988-03-04

Decision Date1988-03-04
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Catheter Technology Corp.. It received FDA 510(k) clearance on 1988-03-04 under 510(k) number K880571. 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 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.

View all 13 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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