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Xre Corp.

FDA 510(k) & PMA Approved Devices — 20 products

Total Devices20
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K973744 UNICATH SP BI-PLANE (MODEL M269 & M289)JAA1997-12-29 View
510(k) K961193 FULL FRAME ZOOM SYSTEMJAA1996-06-17 View
510(k) K960998 XRE COLLIMATORIZW1996-04-03 View
510(k) K945449 UNICATH LLU ANGIOGRAPHIC SYSTEMIZI1995-02-27 View
510(k) K936002 CINEMAC QASIZI1994-09-09 View
510(k) K933460 DVFX, MODEL M256IZI1994-04-07 View
510(k) K924828 BI-NIZI1992-12-17 View
510(k) K923654 POLY DIAGNOST CDXIZI1992-11-20 View
510(k) K913685 UNICATH EP.IZI1991-11-07 View
510(k) K912416 ANGIOGRAPHIC OR FLUOROSCOPIC X-RAY SYSTEMIZI1991-08-28 View
510(k) K892849 UNICATH AIZI1989-08-09 View
510(k) K875184 UNICATH LABIZI1988-01-29 View
510(k) K874113 OMNI DIAGNOSTIXR1987-11-16 View
510(k) K874114 TRAUMA TABLE IIIXR1987-11-16 View
510(k) K854085 OMNI PLANE SYSTEMIXR1985-10-28 View
510(k) K852952 TRAUMA STANDIYB1985-09-26 View
510(k) K853535 TRAUMA TABLEGDC1985-09-11 View
510(k) K850455 QUANTIX CARDIAC ANGIOGRAPHIC SYSTEMIZI1985-05-06 View
510(k) K837515 DENTAL CASSETTE HOLDERS1983-06-28 View
510(k) K761339 RADIAL TRAVEL SPEC. PROCEDURES TABLEIZZ1977-01-05 View
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