FDA 510(k) Applications Submitted by R.J. SLOMOFF

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000065	01/10/2000	CAMLOG CYLINDER IMPLANT SYSTEM	ALTATEC BIOTECHNOLOGIES
K000099	01/13/2000	CAMLOG SCREW IMPLANT SYSTEM	ALTATEC BIOTECHNOLOGIES
K000100	01/13/2000	CAMLOG ROOTFORM IMPLANT SYSTEM	ALTATEC BIOTECHNOLOGIES
K020935	03/22/2002	HEMOCUE GLUCOSE 201 SYSTEM, ARTICLE NUMBER 120706	HEMOCUE, INC.
K961311	04/04/1996	HEMOCUE B-GLUCOSE SYSTEM	HEMOCUE, INC.
K041230	05/10/2004	CLINICAL LABORATORY ANALYZING SYSTEM	HEMOCUE, INC.
K041234	05/10/2004	HEMOCUE HEMOGLOBIN 201DM ANALYZING SYSTEM	HEMOCUE, INC.