MAG RES DIAG DEVI ACCESS CIR POLAR(CP) SPINE COIL— 510(k) K924756

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K924756 for MAG RES DIAG DEVI ACCESS CIR POLAR(CP) SPINE COIL, Substantially Equivalent on 1992-12-30. Applicant: Siemens Medical Solutions USA, Inc..

Clearance details

Applicant: Siemens Medical Solutions USA, Inc.
Product code: Code LNH
Advisory panel: Radiology
Date received: 1992-09-23
Decision date: 1992-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, 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.