The Henry G. Dietz Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - The Henry G. Dietz Co., Inc.
2 devices