FDA 510(k) Application Details - K990561

Device Classification Name	Forceps, Biopsy, Bronchoscope (Rigid)   More FDA Info for this Device
510(K) Number	K990561
Device Name	Forceps, Biopsy, Bronchoscope (Rigid)
Applicant	PILLING WECK SURGICAL 420 DELAWARE DR. FORT WASHINGTON, PA 19034 US Other 510(k) Applications for this Company
Contact	ELIZABETH LAZARO Other 510(k) Applications for this Contact
Regulation Number	874.4680   More FDA Info for this Regulation Number
Classification Product Code	JEK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/22/1999
Decision Date	05/14/1999
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