Mcmurray and Pendergost is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mcmurray and Pendergost - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mcmurray and Pendergost has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1979 to 1979. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Mcmurray and Pendergost Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mcmurray and Pendergost
1 devices