FDA 510(k) Application Details - K052452

Device Classification Name	Nasopharyngoscope (Flexible Or Rigid)   More FDA Info for this Device
510(K) Number	K052452
Device Name	Nasopharyngoscope (Flexible Or Rigid)
Applicant	OLYMPUS MEDICAL SYSTEMS CORPORATION TWO CORPORATE CENTER DR. MELVILLE, NY 11747-9058 US Other 510(k) Applications for this Company
Contact	LAURA STORMS-TYLER 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	09/06/2005
Decision Date	09/21/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review