The Henry G. Dietz Co., Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
The Henry G. Dietz Co., Inc. has 2 FDA 510(k) cleared medical devices. Based in Long Island City, US.
Historical record: 2 cleared submissions from 1991 to 1994. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by The Henry G. Dietz Co., Inc. Filter by specialty or product code using the sidebar.
2 devices