Medical Device Manufacturer · US , Walker , MI

Portex, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1977
20
Total
20
Cleared
0
Denied

Portex, Inc. has 20 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 20 cleared submissions from 1977 to 2004.

Browse the FDA 510(k) cleared devices submitted by Portex, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Portex, Inc.

0 devices
No devices found.
Filters