Q-PORT SYSTEM KIT— 510(k) K894650

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K894650 for Q-PORT SYSTEM KIT, Substantially Equivalent on 1990-03-12. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code LJT
Advisory panel: General Hospital
Date received: 1989-07-24
Decision date: 1990-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, 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.