Ganshorn Medizin Electronic GmbH

Ganshorn Medizin Electronic GmbH holds 2 FDA 510(k) medical device clearances, first cleared 2016, most recent 2024.

Top product codes for Ganshorn Medizin Electronic GmbH

BZG — Anesthesiology1 device
JEH — Anesthesiology1 device

Recent clearances by Ganshorn Medizin Electronic GmbH

K240706 — PowerCube+ Series (3 models)Code JEH·2024-12-09
K160116 — SpiroScoutCode BZG·2016-10-07

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