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FDA 510(k), K092467, VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED
FDA 510(k), K092467, VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED
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510(K) Number: K092467
Device Name: VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED
Manufacturer: ALEXANDER DRUSE
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: HAW
Classification Product Code: 08/12/2009
Date Received: 05/06/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED
Manufacturer: ALEXANDER DRUSE
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: HAW
Classification Product Code: 08/12/2009
Date Received: 05/06/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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