FDA 510(k) Application Details - K024120

Device Classification Name	Kit, Needle, Biopsy   More FDA Info for this Device
510(K) Number	K024120
Device Name	Kit, Needle, Biopsy
Applicant	ALLEGIANCE HEALTHCARE CORP. 1500 WAUKEGAN RD. MPWM-1E MCGAW PARK, IL 60085 US Other 510(k) Applications for this Company
Contact	SHARON NICHOLS Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	FCG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/16/2002
Decision Date	01/15/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review