Dryden Corp. - FDA 510(k) Cleared Devices

Dryden Corp. has 21 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1976 to 1988.

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