FDA 510(k) Application Details - K970756

Device Classification Name	Ventilator, Emergency, Manual (Resuscitator)   More FDA Info for this Device
510(K) Number	K970756
Device Name	Ventilator, Emergency, Manual (Resuscitator)
Applicant	MERCURY MEDICAL 11300-A 49TH ST. NORTH CLEARWATER, FL 34622-4800 US Other 510(k) Applications for this Company
Contact	ARTHUR J WARD 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	03/03/1997
Decision Date	10/31/1997
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