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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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