S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM— 510(k) K882190

Substantially Equivalent

Harbor Medical Devices, Inc.

FDA 510(k) clearance K882190 for S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM, Substantially Equivalent on 1988-06-09. Applicant: Harbor Medical Devices, Inc..

Clearance details

Applicant: Harbor Medical Devices, Inc.
Product code: Code LJT
Advisory panel: General Hospital
Date received: 1988-05-24
Decision date: 1988-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, 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.