ULTIMATE 3000— 510(k) K910839

Substantially Equivalent

Fonar Corp.

FDA 510(k) clearance K910839 for ULTIMATE 3000, Substantially Equivalent on 1991-07-26. Applicant: Fonar Corp..

Clearance details

Applicant: Fonar Corp.
Product code: Code LNH
Advisory panel: Radiology
Date received: 1991-02-27
Decision date: 1991-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

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Adverse events under product code LNH

product code LNH

Death: 11
Injury: 670
Malfunction: 1,460
Other: 2
Total: 2,143

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.