FDA 510(k) Application Details - K022311

Device Classification Name	Rhinoanemometer (Measurement Of Nasal Decongestion)   More FDA Info for this Device
510(K) Number	K022311
Device Name	Rhinoanemometer (Measurement Of Nasal Decongestion)
Applicant	RHINOMETRICS A/S 9675 WEST 95TH ST. MINNEAPOLIS, MN 55344 US Other 510(k) Applications for this Company
Contact	DAN EGGAN 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	07/17/2002
Decision Date	10/04/2002
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