MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)— 510(k) K915567

Name: FDA 510(k) clearance K915567
Creator: U.S. Food and Drug Administration
Published: 1992-05-15

Substantially Equivalent

Fonar Corp.

FDA 510(k) clearance K915567 for MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY), Substantially Equivalent on 1992-05-15. Applicant: Fonar Corp.. Device class: 2.

Clearance details

Applicant: Fonar Corp.
Product code: Code LNH
Device class: Class 2
Regulation: 21 CFR 892.1000
Advisory panel: Radiology
Date received: 1991-12-12
Decision date: 1992-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

Download summary PDF View on FDA.gov ↗

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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.