FDA 510(k) Application Details - K965042

Device Classification Name	Spirometer, Diagnostic   More FDA Info for this Device
510(K) Number	K965042
Device Name	Spirometer, Diagnostic
Applicant	MICRO DIRECT, INC. 840 POWNAL RD. AUBURN, ME 04210 US Other 510(k) Applications for this Company
Contact	DAVID R STASZAK 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	12/17/1996
Decision Date	06/17/1997
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