FDA 510(k) Application Details - K072887

Device Classification Name	Exerciser, Powered   More FDA Info for this Device
510(K) Number	K072887
Device Name	Exerciser, Powered
Applicant	ALTER-G, INC. 1090A O'BRIEN DRIVE MENLO PARK, CA 94025 US Other 510(k) Applications for this Company
Contact	GLEN MANGSETH Other 510(k) Applications for this Contact
Regulation Number	890.5380   More FDA Info for this Regulation Number
Classification Product Code	BXB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/10/2007
Decision Date	01/25/2008
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