Medical Device Manufacturer · DE , Niederlauer

Ganshorn Medizin Electronic GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ganshorn Medizin Electronic GmbH Anesthesiology ✕
2 devices
1-2 of 2
Cleared Dec 09, 2024
PowerCube+ Series (PowerCube Body+)
K240706 · JEH
Anesthesiology · 270d
Cleared Oct 07, 2016
SpiroScout
K160116 · BZG
Anesthesiology · 262d
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