FDA 510(k) Applications Submitted by BETH A ROCHETTE

FDA 510(k) Number Submission Date Device Name Applicant
K971137 03/28/1997 BARD RAPIDFIRE MULTIPLE BAND LIGATOR C.R. BARD, INC.
K962178 06/06/1996 BARD TIGER GUIDEWIRE MODEL 000540 C.R. BARD, INC.
K963484 09/03/1996 BARD HIGH FLOW PAPILLOTOME BARD INTERVENTIONAL PRODUCTS DIV.
K964780 11/27/1996 BARD DIRECTOR GUIDEWIRE (000560) C.R. BARD, INC.


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