FDA 510(k) Application Details - K032852

Device Classification Name	Compressor, Cardiac, External   More FDA Info for this Device
510(K) Number	K032852
Device Name	Compressor, Cardiac, External
Applicant	REVIVANT CORP. 775 PALOMAR AVE. SUNNYVALE, CA 94085 US Other 510(k) Applications for this Company
Contact	BOB H KATZ Other 510(k) Applications for this Contact
Regulation Number	870.5200   More FDA Info for this Regulation Number
Classification Product Code	DRM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/12/2003
Decision Date	11/12/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review