FDA 510(k) Application Details - K031643

Device Classification Name	Spirometer, Diagnostic   More FDA Info for this Device
510(K) Number	K031643
Device Name	Spirometer, Diagnostic
Applicant	SDI DIAGNOSTICS, INC. 10 HAMPDEN DR. EASTON, MA 02375 US Other 510(k) Applications for this Company
Contact	MICHAEL J BOYLE Other 510(k) Applications for this Contact
Regulation Number	868.1840   More FDA Info for this Regulation Number
Classification Product Code	BZG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/27/2003
Decision Date	12/09/2003
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