FDA 510(k) Applications Submitted by BARD INTERVENTIONAL PRODUCTS DIV.

FDA 510(k) Number Submission Date Device Name Applicant
K963484 09/03/1996 BARD HIGH FLOW PAPILLOTOME BARD INTERVENTIONAL PRODUCTS DIV.
K982557 07/22/1998 BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES BARD INTERVENTIONAL PRODUCTS DIV.


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