FDA 510(k) Application Details - K070672

Device Classification Name	Table, Physical Therapy, Multi Function   More FDA Info for this Device
510(K) Number	K070672
Device Name	Table, Physical Therapy, Multi Function
Applicant	METEK GMBH STAMMWEG 8 LEINEFELDE 37327 DE Other 510(k) Applications for this Company
Contact	STEFAN ZIEGENFUB Other 510(k) Applications for this Contact
Regulation Number	890.5880   More FDA Info for this Regulation Number
Classification Product Code	JFB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/12/2007
Decision Date	06/26/2007
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	Y
Expedited Review