FDA 510(k) Application Details - K955711

Device Classification Name	Dilator, Nasal   More FDA Info for this Device
510(K) Number	K955711
Device Name	Dilator, Nasal
Applicant	CNS, INC. P.O. BOX 39802 MINNEAPOLIS, MN 55439-0802 US Other 510(k) Applications for this Company
Contact	M.W. (ANDY) ANDERSON Other 510(k) Applications for this Contact
Regulation Number	874.3900   More FDA Info for this Regulation Number
Classification Product Code	LWF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/18/1995
Decision Date	05/30/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review