FDA 510(k) Application Details - K022636

Device Classification Name	Plethysmograph, Volume   More FDA Info for this Device
510(K) Number	K022636
Device Name	Plethysmograph, Volume
Applicant	MORGAN SCIENTIFIC, INC. 151 ESSEX ST. HAVERHILL, MA 01832 US Other 510(k) Applications for this Company
Contact	PATRICK F MORGAN Other 510(k) Applications for this Contact
Regulation Number	868.1760   More FDA Info for this Regulation Number
Classification Product Code	JEH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/08/2002
Decision Date	01/13/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review