FDA 510(k) Application Details - K131023

Device Classification Name	Conserver, Oxygen   More FDA Info for this Device
510(K) Number	K131023
Device Name	Conserver, Oxygen
Applicant	MEDICAL PRODUCTS, LLC 7437 OAKLANDON RD. INDIANAPOLIS, IN 46236 US Other 510(k) Applications for this Company
Contact	DAVID MCGILL Other 510(k) Applications for this Contact
Regulation Number	868.5905   More FDA Info for this Regulation Number
Classification Product Code	NFB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/12/2013
Decision Date	10/11/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review