FDA 510(k) Application Details - K093694

Device Classification Name	System, Thermal Regulating   More FDA Info for this Device
510(K) Number	K093694
Device Name	System, Thermal Regulating
Applicant	GERATHERM MEDICAL AG SCHWARZWALDSTRASSE 5 TUTTLIGEN 78532 DE Other 510(k) Applications for this Company
Contact	ANDREA PECSI Other 510(k) Applications for this Contact
Regulation Number	870.5900   More FDA Info for this Regulation Number
Classification Product Code	DWJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/30/2009
Decision Date	09/20/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review