Xre Corp.
Xre Corp. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1997.
Top product codes for Xre Corp.
Recent clearances by Xre Corp.
- K973744 — UNICATH SP BI-PLANE (MODEL M269 & M289)
- K961193 — FULL FRAME ZOOM SYSTEM
- K960998 — XRE COLLIMATOR
- K945449 — UNICATH LLU ANGIOGRAPHIC SYSTEM
- K936002 — CINEMAC QAS
- K933460 — DVFX, MODEL M256
- K924828 — BI-N
- K923654 — POLY DIAGNOST CDX
- K913685 — UNICATH EP.
- K912416 — ANGIOGRAPHIC OR FLUOROSCOPIC X-RAY SYSTEM
- K892849 — UNICATH A
- K875184 — UNICATH LAB
- K874113 — OMNI DIAGNOST
- K874114 — TRAUMA TABLE II
- K854085 — OMNI PLANE SYSTEM
- K852952 — TRAUMA STAND
- K853535 — TRAUMA TABLE
- K850455 — QUANTIX CARDIAC ANGIOGRAPHIC SYSTEM
- K837515 — DENTAL CASSETTE HOLDERS
- K761339 — RADIAL TRAVEL SPEC. PROCEDURES TABLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.