FDA 510(k) Applications Submitted by PENTAPHARM LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K042760 10/05/2004 PEFAKIT APC-R FACTOR V LEIDEN CONTROLS PENTAPHARM LTD.
K042762 10/05/2004 PEFAKIT APC-R FACTOR V LEIDEN PENTAPHARM LTD.


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