MODIFIED MATERIAL USED IN INFUSION T— 510(k) K893909

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K893909 for MODIFIED MATERIAL USED IN INFUSION T, Substantially Equivalent on 1989-08-25. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code FPA
Advisory panel: General Hospital
Date received: 1989-05-30
Decision date: 1989-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

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.