Zurich Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zurich Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Zurich Pressure Guidewire System Model 100
1
Total
1
Cleared
0
Denied
Zurich Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zurich Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Zurich Medical, Inc.
1 devices