Diter Elektroniikka OY

Diter Elektroniikka OY holds 1 FDA 510(k) medical device clearance, cleared in 1990.

Top product codes for Diter Elektroniikka OY

IMI — Physical Medicine1 device

Recent clearances by Diter Elektroniikka OY

K901950 — DITER ULTRASONIC S 3000Code IMI·1990-07-27

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