Ge Dec Medical Systems
Ge Dec Medical Systems holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2000.
Top product codes for Ge Dec Medical Systems
Recent clearances by Ge Dec Medical Systems
- K000221 — SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM
- K993687 — UROVIEW 2800
- K992506 — MINI 6800 DIGITAL MOBILE C-ARM
- K974355 — INTERVENTIONAL MOBILE DIGITAL IMAGING SYSTEM (HEREIN CALLED IMDIS)
- K970063 — SERIES 7600 MOBILE DIGITAL C-ARM
- K963952 — SERIES 9600 MOBILE DIGITAL IMAGING SYSTEM
- K950781 — COMPACT 7600
- K951765 — SERIES 6600 DIGITAL MOBILE C-ARM
- K940295 — UROVIEW MODEL 2600
- K936136 — UROVIEW SYSTEMS TOMOGRAPHY OPTION SOFTWARE
Data sourced from openFDA. This site is unofficial and independent of the FDA.