FDA 510(k) Application Details - DEN000004

Device Classification Name	Device,Heimlich Maneuver Assist   More FDA Info for this Device
510(K) Number	DEN000004
Device Name	Device,Heimlich Maneuver Assist
Applicant	MAET INDUSTRIES, INC. 4215 RENOAK COURT MISSISSAUGA, ONTARIO L5C 4K3 CA Other 510(k) Applications for this Company
Contact	WAYNE WITBECK Other 510(k) Applications for this Contact
Regulation Number	868.5115   More FDA Info for this Regulation Number
Classification Product Code	MZT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/28/2000
Decision Date	02/29/2000
Decision	DENG -
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review