ULTRASYSTEM LINSCAN PROBE— 510(k) K842811

Substantially Equivalent

Kelley Development Corp.

FDA 510(k) clearance K842811 for ULTRASYSTEM LINSCAN PROBE, Substantially Equivalent on 1984-09-17. Applicant: Kelley Development Corp..

Clearance details

Applicant: Kelley Development Corp.
Product code: Code IYO
Advisory panel: Radiology
Date received: 1984-07-18
Decision date: 1984-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.