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FDA 510(k) Applications Submitted by ARTEMIS MEDICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020024
01/03/2002
CARIS MINITOME BIOPSY INSTRUMENT
ARTEMIS MEDICAL, INC.
K032217
07/21/2003
14G CORMARK BIOPSY SITE IDENTIFIER
ARTEMIS MEDICAL, INC.
K003777
12/07/2000
CARIS SITE MARKER
ARTEMIS MEDICAL, INC.
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