FDA 510(k) Application Details - K992310

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K992310
Device Name	Wheelchair, Mechanical
Applicant	RUPIANI MEDICAL 98 RUE ALEXANDRE DUMAS VAULX EN VELIN 69120 FR Other 510(k) Applications for this Company
Contact	JEAN-MARIE MANGENOT Other 510(k) Applications for this Contact
Regulation Number	890.3850   More FDA Info for this Regulation Number
Classification Product Code	IOR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/09/1999
Decision Date	11/02/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review