FDA 510(k) Application Details - K010252

Device Classification Name	Table, Physical Therapy, Multi Function   More FDA Info for this Device
510(K) Number	K010252
Device Name	Table, Physical Therapy, Multi Function
Applicant	MAGNUM EQUIPMENT L.L.C. 7222 W. MELROSE LN. OKLAHOMA CITY, OK 73127 US Other 510(k) Applications for this Company
Contact	MONTE REGAL 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	01/26/2001
Decision Date	04/26/2001
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