FDA 510(k) Application Details - K973624

Device Classification Name	Bed, Flotation Therapy, Powered   More FDA Info for this Device
510(K) Number	K973624
Device Name	Bed, Flotation Therapy, Powered
Applicant	AIR MED ASSIST PRODUCTS P.O. BOX 154 (FEDERAL BLDG.) 65 N. MAIN, STE TOOLE, UT 84074-0154 US Other 510(k) Applications for this Company
Contact	JOHN E LINCOLN Other 510(k) Applications for this Contact
Regulation Number	890.5170   More FDA Info for this Regulation Number
Classification Product Code	IOQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/23/1997
Decision Date	01/21/1998
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