FDA 510(k) Application Details - K000406

Device Classification Name	Rhinoanemometer (Measurement Of Nasal Decongestion)   More FDA Info for this Device
510(K) Number	K000406
Device Name	Rhinoanemometer (Measurement Of Nasal Decongestion)
Applicant	RHINOMETRICS A/S 555 13TH ST. N.W. WASHINGTON, DC 20004-1109 US Other 510(k) Applications for this Company
Contact	HOWARD M HOLSTEIN Other 510(k) Applications for this Contact
Regulation Number	868.1800   More FDA Info for this Regulation Number
Classification Product Code	BXQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/07/2000
Decision Date	04/17/2000
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