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FDA 510(k) Applications Submitted by KRIS TEICH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K963328
08/23/1996
AMS AMBICOR PENILE PROSTHESIS
AMERICAN MEDICAL SYSTEMS, INC.
K030019
01/03/2003
MODIFICATION TO HI-TORQUE WHISPER GUIDEWIRE
GUIDANT CORP.
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