FDA 510(k) Application Details - K960861

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K960861
Device Name	Ventilator, Continuous, Facility Use
Applicant	CORE-M, INC. 214 LINCOLN ST. ALLSTON, MA 02134 US Other 510(k) Applications for this Company
Contact	C. LAWERENCE CHRISTMAN Other 510(k) Applications for this Contact
Regulation Number	868.5895   More FDA Info for this Regulation Number
Classification Product Code	CBK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/01/1996
Decision Date	08/19/1996
Decision	ST - Substantially Equivalent - Subject to Tracking Reg.
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review