FDA 510(k) Application Details - K023793

Device Classification Name	Ventilator, Emergency, Manual (Resuscitator)   More FDA Info for this Device
510(K) Number	K023793
Device Name	Ventilator, Emergency, Manual (Resuscitator)
Applicant	PORTEX, INC. 10 BOWMAN DR. KEENE, NH 03431 US Other 510(k) Applications for this Company
Contact	CINDY ENGELHARDT Other 510(k) Applications for this Contact
Regulation Number	868.5915   More FDA Info for this Regulation Number
Classification Product Code	BTM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/13/2002
Decision Date	02/11/2003
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