FDA 510(k) Application Details - K983187

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K983187
Device Name	Instrument, Biopsy
Applicant	MEDSOL CORP. 4 WASHINGTON SQ. VILLAGE 8P NEW YORK, NY 10012 US Other 510(k) Applications for this Company
Contact	ALEC S GOLDENBERG Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	KNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/11/1998
Decision Date	12/10/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review