FDA 510(k) Application Details - K993921

Device Classification Name	Spirometer, Diagnostic   More FDA Info for this Device
510(K) Number	K993921
Device Name	Spirometer, Diagnostic
Applicant	NDD MEDICAL TECHNOLOGIES 17 PROGRESS ANENUE CHELMSFORD, MA 01824 US Other 510(k) Applications for this Company
Contact	OSCAR KAELIN 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	11/18/1999
Decision Date	05/23/2000
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