FDA 510(k) Application Details - K980281

Device Classification Name	Light Source, Endoscope, Xenon Arc   More FDA Info for this Device
510(K) Number	K980281
Device Name	Light Source, Endoscope, Xenon Arc
Applicant	WELCH ALLYN, INC. 4619 JORDAN RD. SKANEATELES FALLS, NY 13153-0187 US Other 510(k) Applications for this Company
Contact	KATHY LOWTHER Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	GCT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/26/1998
Decision Date	02/27/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review