FDA 510(k) Application Details - K993851

Device Classification Name	Motor, Drill, Pneumatic   More FDA Info for this Device
510(K) Number	K993851
Device Name	Motor, Drill, Pneumatic
Applicant	SODEMSYSTEMS 110, CH. DU PONT-DU-CENTENAIRE GENEVA, SWITZERLAND CH 1228 CH Other 510(k) Applications for this Company
Contact	DANIEL BACCINO Other 510(k) Applications for this Contact
Regulation Number	882.4370   More FDA Info for this Regulation Number
Classification Product Code	HBB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/12/1999
Decision Date	12/27/1999
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