FDA 510(k) Application Details - K984031

Device Classification Name	Spirometer, Diagnostic   More FDA Info for this Device
510(K) Number	K984031
Device Name	Spirometer, Diagnostic
Applicant	SCHILLER AG ALTGASSE 68 BAAR CH-6341 CH Other 510(k) Applications for this Company
Contact	MARKUS BUETLER 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	11/12/1998
Decision Date	04/30/1999
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