MODIFIED QUINTON SINGLE LUMEN CATHETER— 510(k) K896252

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K896252 for MODIFIED QUINTON SINGLE LUMEN CATHETER, Substantially Equivalent on 1990-01-29. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code MPB
Advisory panel: Gastroenterology, Urology
Date received: 1989-10-30
Decision date: 1990-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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Adverse events under product code MPB

product code MPB

Death: 18
Malfunction: 1,042
Total: 1,060

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.