Medical Device Manufacturer · DK , Glostrop

Scandimed. A.S.

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

Scandimed. A.S. — FDA 510(k) Submissions

Scandimed. A.S. has submitted 2 FDA 510(k) premarket notifications since 2003, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscopic Injection Needle, Gastroenterology-urology, Ligator, Esophageal . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Gastroenterology & Urology 2