FDA 510(k) Application Details - K954914

Device Classification Name	Dilator, Nasal   More FDA Info for this Device
510(K) Number	K954914
Device Name	Dilator, Nasal
Applicant	CNS, INC. 1250 PARK RD. CHANHASSEN, MN 55317 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	10/26/1995
Decision Date	02/27/1996
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