FDA 510(k) Applications Submitted by RALPH FLATAU

FDA 510(k) Number Submission Date Device Name Applicant
K992392 07/19/1999 RTLX INFIMED, INC.
K992794 08/19/1999 STINGRAY DR, MODEL 1 INFIMED, INC.
K992575 08/02/1999 CARDIOVASCULAR WORKSTATION, MODEL CWS 5000/CWS 3000 INFIMED, INC.
K012490 08/03/2001 ORION DIGITAL IMAGING SYSTEM INFIMED, INC.


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