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

Penlon, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1980 to 1994.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.