FDA 510(k), K160811, CRW STEREOTACTIC SYSTEM

FDA 510(k), K160811, CRW STEREOTACTIC SYSTEM

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510(K) Number: K160811
Device Name: CRW STEREOTACTIC SYSTEM
Manufacturer:
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: HAW
Date Received: 03/24/2016
Decision Date: 12/06/2016
Regulation Medical Specialty: Neurology
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