Quantel Derma GmbH is one of 22265 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quantel Derma GmbH - FDA 510(k) Cleared Devices
Recent clearances: EXELO2, MODEL 4010, LEDA
2
Total
2
Cleared
0
Denied
Quantel Derma GmbH has 2 FDA 510(k) cleared medical devices. Based in Bozeman, US.
Historical record: 2 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Quantel Derma GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Quantel Derma GmbH
2 devices