Mermaid Medical A/S is one of 86 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Mermaid Medical A/S - FDA 510(k) Cleared Devices
Recent clearances: M-Biopsy Semi-Automatic Biopsy Instrument M-Biopsy Coaxial Introducer Needle for Sem
1
Total
1
Cleared
0
Denied
Mermaid Medical A/S has 1 FDA 510(k) cleared medical devices. Based in Stenloese, DK.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mermaid Medical A/S Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Registrar Corp. as regulatory consultant.
FDA 510(k) Regulatory Record - Mermaid Medical A/S
1 devices