CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM— 510(k) K880571

Substantially Equivalent

Catheter Technology Corp.

FDA 510(k) clearance K880571 for CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, Substantially Equivalent on 1988-03-04. Applicant: Catheter Technology Corp..

Clearance details

Applicant: Catheter Technology Corp.
Product code: Code LJT
Advisory panel: General Hospital
Date received: 1988-02-10
Decision date: 1988-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Adverse events under product code LJT

product code LJT

Death: 234
Injury: 6,468
Malfunction: 5,326
Other: 2
Total: 12,030

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.