Par Medizintechnik GmbH & Co. KG

Par Medizintechnik GmbH & Co. KG holds 1 FDA 510(k) medical device clearance, cleared in 2017.

Top product codes for Par Medizintechnik GmbH & Co. KG

DXN — Cardiovascular1 device

Recent clearances by Par Medizintechnik GmbH & Co. KG

K170966 — TONOPORT VICode DXN·2017-06-14

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