FDA 510(k), K972324, LEKSELL STEREOTACTIC SYSTEM

FDA 510(k), K972324, LEKSELL STEREOTACTIC SYSTEM

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510(K) Number: K972324
Device Name: LEKSELL STEREOTACTIC SYSTEM
Manufacturer: ELEKTA INSTRUMENT AB
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: HAW
Date Received: 06/23/1997
Decision Date: 03/02/1998
Regulation Medical Specialty: Neurology

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