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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