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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.
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