This page includes the latest FDA filings for Xre Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
XRE CORP. | UNICATH SP BI-PLANE (MODEL M269 & M289) | 1997-12-29 |
XRE CORP. | FULL FRAME ZOOM SYSTEM | 1996-06-17 |
XRE CORP. | XRE COLLIMATOR | 1996-04-03 |
XRE CORP. | UNICATH LLU ANGIOGRAPHIC SYSTEM | 1995-02-27 |
XRE CORP. | CINEMAC QAS | 1994-09-09 |
XRE CORP. | DVFX, MODEL M256 | 1994-04-07 |
XRE CORP. | BI-N | 1992-12-17 |
XRE CORP. | POLY DIAGNOST CDX | 1992-11-20 |
XRE CORP. | UNICATH EP. | 1991-11-07 |
XRE CORP. | ANGIOGRAPHIC OR FLUOROSCOPIC X-RAY SYSTEM | 1991-08-28 |
XRE CORP. | UNICATH A | 1989-08-09 |
XRE CORP. | UNICATH LAB | 1988-01-29 |
XRE CORP. | TRAUMA TABLE II | 1987-11-16 |
XRE CORP. | OMNI DIAGNOST | 1987-11-16 |
XRE CORP. | OMNI PLANE SYSTEM | 1985-10-28 |
XRE CORP. | TRAUMA STAND | 1985-09-26 |
XRE CORP. | TRAUMA TABLE | 1985-09-11 |
XRE CORP. | QUANTIX CARDIAC ANGIOGRAPHIC SYSTEM | 1985-05-06 |
XRE CORP. | DENTAL CASSETTE HOLDERS | 1983-06-28 |