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FDA 510(k) Applications Submitted by JOSHUA R LEVY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081760
06/20/2008
RSVP PHANTOM PELVIS, MODEL TLP260
THE PHANTOM LABORATORY, INC.
K002840
09/12/2000
MARKS REFERENCE PHANTOM, MEASURE REFERENCE PHANTOM
THE PHANTOM LABORATORY, INC.
K082909
09/30/2008
RSVP HALF SPHERE PHANTOM, MODEL DDP010
THE PHANTOM LABORATORY, INC.
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