FDA 510(k) Application Details - K990445

Device Classification Name	Massager, Therapeutic, Electric   More FDA Info for this Device
510(K) Number	K990445
Device Name	Massager, Therapeutic, Electric
Applicant	LPG USA, INC. 3101 NORTH FEDERAL HWY. #300 FORT LAUDERDALE, FL 33306 US Other 510(k) Applications for this Company
Contact	JOCELYNE ROLLAND Other 510(k) Applications for this Contact
Regulation Number	890.5660   More FDA Info for this Regulation Number
Classification Product Code	ISA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/10/1999
Decision Date	01/18/2000
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