Midmark Diagnostics Group

Midmark Diagnostics Group holds 1 FDA 510(k) medical device clearance, cleared in 2007.

Top product codes for Midmark Diagnostics Group

MWI — Cardiovascular1 device

Recent clearances by Midmark Diagnostics Group

K072516 — MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITORCode MWI·2007-10-18

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