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FDA 510(k) Applications Submitted by XRE CORP.
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.
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