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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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