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Xre Corp.

20 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
UNICATH SP BI-PLANE (MODEL M269 & M289) (K973744)Xre Corp.1997-12-29
FULL FRAME ZOOM SYSTEM (K961193)Xre Corp.1996-06-17
XRE COLLIMATOR (K960998)Xre Corp.1996-04-03
UNICATH LLU ANGIOGRAPHIC SYSTEM (K945449)Xre Corp.1995-02-27
CINEMAC QAS (K936002)Xre Corp.1994-09-09
DVFX, MODEL M256 (K933460)Xre Corp.1994-04-07
BI-N (K924828)Xre Corp.1992-12-17
POLY DIAGNOST CDX (K923654)Xre Corp.1992-11-20
UNICATH EP. (K913685)Xre Corp.1991-11-07
ANGIOGRAPHIC OR FLUOROSCOPIC X-RAY SYSTEM (K912416)Xre Corp.1991-08-28
UNICATH A (K892849)Xre Corp.1989-08-09
UNICATH LAB (K875184)Xre Corp.1988-01-29
OMNI DIAGNOST (K874113)Xre Corp.1987-11-16
TRAUMA TABLE II (K874114)Xre Corp.1987-11-16
OMNI PLANE SYSTEM (K854085)Xre Corp.1985-10-28
TRAUMA STAND (K852952)Xre Corp.1985-09-26
TRAUMA TABLE (K853535)Xre Corp.1985-09-11
QUANTIX CARDIAC ANGIOGRAPHIC SYSTEM (K850455)Xre Corp.1985-05-06
DENTAL CASSETTE HOLDERS (K837515)Xre Corp.1983-06-28
RADIAL TRAVEL SPEC. PROCEDURES TABLE (K761339)Xre Corp.1977-01-05

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