FDA 510(k) Application Details - K030572

Device Classification Name	Nasopharyngoscope (Flexible Or Rigid)   More FDA Info for this Device
510(K) Number	K030572
Device Name	Nasopharyngoscope (Flexible Or Rigid)
Applicant	HENKE SASS WOLF OF AMERICA, INC. 203 MAIN STREET, PMB 166 FLEMINGTON, NJ 08822 US Other 510(k) Applications for this Company
Contact	LYNETTE HOWARD Other 510(k) Applications for this Contact
Regulation Number	874.4760   More FDA Info for this Regulation Number
Classification Product Code	EOB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/24/2003
Decision Date	04/01/2003
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