Mitsubishi Heavy Industries, Ltd.

Mitsubishi Heavy Industries, Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2007, most recent 2015.

Top product codes for Mitsubishi Heavy Industries, Ltd.

IYE — Radiology3 devices

Recent clearances by Mitsubishi Heavy Industries, Ltd.

K152867 — MHI-TM2000 Linear Accelerator System, VERO, ImavisCode IYE·2015-10-21
K122450 — MHI-TM2000 LINEAR ACCELERATOR SYSTEM VERO IMAVISCode IYE·2012-10-03
K072047 — MHI-TM2000 LINEAR ACCELERATOR SYSTEMCode IYE·2007-08-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.