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FDA 510(k) Applications Submitted by ELIZABETH DOLAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020667
03/01/2002
CODMAN HAKIM SHUNT SYSTEMS
Codman & Shurtleff, Inc.
K031123
04/09/2003
CODMAN BACTISEAL BARIUM STRIPED CATHETERS
Codman & Shurtleff, Inc.
K041518
06/07/2004
CODMAN DURAFORM DURAL GRAFT IMPLANT
Codman & Shurtleff, Inc.
K023566
10/23/2002
CODMAN ISOCOOL BIPOLAR FORCEPS
Codman & Shurtleff, Inc.
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