FDA 510(k) Application Details - K960402

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K960402
Device Name	Wheelchair, Mechanical
Applicant	METRO-CARE 1550 NORTH FEDERAL HWY., #4 DELRAY BEACH, FL 33483 US Other 510(k) Applications for this Company
Contact	JODY GLADSTONE 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	01/29/1996
Decision Date	02/16/1996
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