FDA 510(k) Application Details - K103392

Device Classification Name	Conserver, Oxygen   More FDA Info for this Device
510(K) Number	K103392
Device Name	Conserver, Oxygen
Applicant	INOVO, INC. 2975 S. HORSESHOE DRIVE SUITE 600 NAPLES, FL 34104 US Other 510(k) Applications for this Company
Contact	MICHAEL T DILDINE 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	11/19/2010
Decision Date	12/17/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review