FDA 510(k) Application Details - K954378

Device Classification Name	Vehicle, Motorized 3-Wheeled   More FDA Info for this Device
510(K) Number	K954378
Device Name	Vehicle, Motorized 3-Wheeled
Applicant	AEROTEK P.O. BOX 394 RENFREW, ONTARIO K7V4A6 CA Other 510(k) Applications for this Company
Contact	JANET OSBORNE Other 510(k) Applications for this Contact
Regulation Number	890.3800   More FDA Info for this Regulation Number
Classification Product Code	INI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/19/1995
Decision Date	07/25/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review