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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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