Medical Device Manufacturer · US , Plymouth , MN

Zurich Medical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2019

Recent clearances: Zurich Pressure Guidewire System Model 100

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Zurich Medical, Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Aug 14, 2019

Zurich Pressure Guidewire System Model 100

Cardiovascular · 134d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Jun 04, 2026