FDA 510(k) Applications Submitted by MICHAEL CARROLL

FDA 510(k) Number Submission Date Device Name Applicant
K020379 02/05/2002 PPD BALLOON DILATATION CATHETER TELEMED SYSTEMS, INC.
K010412 02/12/2001 FLEXIBLE ENDOSCOPIC SCISSORS TELEMED SYSTEMS, INC.
K013737 11/13/2001 MODIFICATION TO: 3-LUMEN DURALON OCCLUSION BALLOON TELEMED SYSTEMS, INC.


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