FDA 510(k) Applications Submitted by WAYNE V LOOMER

FDA 510(k) Number Submission Date Device Name Applicant
K960998 03/12/1996 XRE COLLIMATOR XRE CORP.
K961193 03/21/1996 FULL FRAME ZOOM SYSTEM XRE CORP.
K973744 10/01/1997 UNICATH SP BI-PLANE (MODEL M269 & M289) XRE CORP.
K984414 12/10/1998 XRE COLLIMATOR WITH SPECTRAL FILTER TREX MEDICAL CORP.


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