FDA 510(k) Application Details - K991267

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K991267
Device Name	Neurological Stereotaxic Instrument
Applicant	OHIO MEDICAL INSTRUMENT CO., INC. 4900 CHARLEMAR DR. CINCINNATI, OH 45227 US Other 510(k) Applications for this Company
Contact	KENNETH B MILLER Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	HAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/13/1999
Decision Date	07/12/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review