FDA 510(k) Application Details - K964719

Device Classification Name	Ventilator, Emergency, Manual (Resuscitator)   More FDA Info for this Device
510(K) Number	K964719
Device Name	Ventilator, Emergency, Manual (Resuscitator)
Applicant	HUDSON RESPIRATORY CARE, INC. 27711 DIAZ RD. P.O. BOX 9020 TEMECULA, CA 92589-9020 US Other 510(k) Applications for this Company
Contact	ARDEN P MORLEY 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	11/25/1996
Decision Date	02/21/1997
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