Medical Device Manufacturer · US , Washington , DC

Huttinger Medizintechnik GmbH & CO KG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

Recent clearances: MAGNA TEK ESU-400, PY30, PY60, PY80

2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Huttinger Medizintechnik GmbH & CO KG General & Plastic Surgery ✕

2 devices
1-2 of 2
Filters