Dafoe & Dafoe, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dafoe & Dafoe, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Dafoe & Dafoe, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1980 to 1982. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Dafoe & Dafoe, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dafoe & Dafoe, Inc.
4 devices