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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