FDA 510(k) Applications Submitted by WENDY A URTEL

FDA 510(k) Number	Submission Date	Device Name	Applicant
K994309	12/21/1999	SOLO ORTHO 2	SYBRON DENTAL SPECIALTIES, INC.
K981023	03/19/1998	KLEENASEPTIC	METREX RESEARCH CORP.
K981448	04/22/1998	KERR HARD DENTURE RELINE MATERIAL	SYBRON DENTAL SPECIALTIES, INC.
K974105	10/31/1997	KERR COMPOMER	SYBRON DENTAL SPECIALTIES, INC.