FDA 510(k) Application Details - K011329

Device Classification Name	Rhinoanemometer (Measurement Of Nasal Decongestion)   More FDA Info for this Device
510(K) Number	K011329
Device Name	Rhinoanemometer (Measurement Of Nasal Decongestion)
Applicant	E. BENSON HOOD LAB, INC. 575 WASHINGTON ST. PEMBROKE, MA 02359 US Other 510(k) Applications for this Company
Contact	LEWIS MARTEN 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	05/01/2001
Decision Date	07/26/2002
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