Huttinger Medizintechnik GmbH & CO KG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Huttinger Medizintechnik GmbH & CO KG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Huttinger Medizintechnik GmbH & CO KG has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 1995 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Huttinger Medizintechnik GmbH & CO KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Huttinger Medizintechnik GmbH & CO KG
2 devices