FDA 510(k) Application Details - K080545

Device Classification Name	Exerciser, Measuring   More FDA Info for this Device
510(K) Number	K080545
Device Name	Exerciser, Measuring
Applicant	ACTIGRAPH, LLC 15 W. MAIN. ST PENSACOLA, FL 32502 US Other 510(k) Applications for this Company
Contact	JOHN SCHEIDER Other 510(k) Applications for this Contact
Regulation Number	890.5360   More FDA Info for this Regulation Number
Classification Product Code	ISD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/27/2008
Decision Date	07/24/2008
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