K-AID— 510(k) K820150

Substantially Equivalent

Sytek Laboratories

FDA 510(k) clearance K820150 for K-AID, Substantially Equivalent on 1982-01-29. Applicant: Sytek Laboratories.

Clearance details

Applicant: Sytek Laboratories
Product code: Code KPO
Advisory panel: Gastroenterology, Urology
Date received: 1982-01-19
Decision date: 1982-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KPO

product code KPO

Death: 14
Malfunction: 775
Other: 20
Total: 809

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.