FDA 510(k) Application Details - K993194

Device Classification Name	Ventilator, Emergency, Manual (Resuscitator)   More FDA Info for this Device
510(K) Number	K993194
Device Name	Ventilator, Emergency, Manual (Resuscitator)
Applicant	RUSCH, INC. 2450 MEADOWBROOK PKWY. DULUTH, GA 30096 US Other 510(k) Applications for this Company
Contact	RONALD YOUNG 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	09/23/1999
Decision Date	03/24/2000
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