FDA 510(k) Application Details - K072011

Device Classification Name	Unit, Liquid-Oxygen, Portable   More FDA Info for this Device
510(K) Number	K072011
Device Name	Unit, Liquid-Oxygen, Portable
Applicant	COPD PARTNERS, INC. 3460 POINTE CREEK CT. SUITE 102 BONITA SPRINGS, FL 34134-2015 US Other 510(k) Applications for this Company
Contact	PAUL DRYDEN Other 510(k) Applications for this Contact
Regulation Number	868.5655   More FDA Info for this Regulation Number
Classification Product Code	BYJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/23/2007
Decision Date	10/18/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review