Eigen
Eigen holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2023.
Top product codes for Eigen
Recent clearances by Eigen
- K222222 — Artemis, Artemis TPO, Artemis MX
- K173744 — ProFuse CAD
- K162474 — Artemis
- K063846 — EIGEN DSA 2000
- K933115 — DIGITAL DISK RECORDER
- K924164 — DIGITAL DISK RECORDER W/DUALPATH ARCHIVE/30-60 OPT
- K923585 — DIGITAL FLUORO STORE
- K913012 — DIGITAL FLUORO STORE(DFS) W/NUMERICAL SUFFIXES
- K905111 — DIGITAL DISK RECORDER(DDR) W/NUMERICAL SUFFIXES
- K903821 — PSC-1 W/OTHER NUMERICAL
- K902927 — DIGITAL PHOTOSPOT
- K901956 — DIGITAL 8 W/OTHER NUMERICAL SUFFIXES (1-9, ETC.)
- K890745 — SC-1000 WITH SUFFIXES (SCAN CONVERTER)
- K882175 — HR-2000 W/SUFFIXES B,C,D, CARDIO & DIGI LOOP, DDVP
- K882176 — VTR-12
- K882184 — HR-1000 W/SUFFIXES (B,C OR D)
Data sourced from openFDA. This site is unofficial and independent of the FDA.