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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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