FDA 510(k) Application Details - K993088

Device Classification Name	Generator, Oxygen, Portable   More FDA Info for this Device
510(K) Number	K993088
Device Name	Generator, Oxygen, Portable
Applicant	PURITAN BENNETT CORP. 2200 FARADAY AVE. CARLSBAD, CA 92008 US Other 510(k) Applications for this Company
Contact	TONY KEAVENEY Other 510(k) Applications for this Contact
Regulation Number	868.5440   More FDA Info for this Regulation Number
Classification Product Code	CAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/1999
Decision Date	10/08/1999
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