FDA 510(k) Application Details - K042610

Device Classification Name	Cream, Nasal, Topical, Mechanical Allergen Particle Barrier   More FDA Info for this Device
510(K) Number	K042610
Device Name	Cream, Nasal, Topical, Mechanical Allergen Particle Barrier
Applicant	DR. THEISS NATURWAREN GMBH 815 CONNECTICUT AVE., NW SUITE 800 WASHINGTON, DC 20006 US Other 510(k) Applications for this Company
Contact	STUART PORTNOY Other 510(k) Applications for this Contact
Regulation Number	880.5045   More FDA Info for this Regulation Number
Classification Product Code	NUP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/24/2004
Decision Date	05/16/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review