Mckeon Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mckeon Products - FDA 510(k) Cleared Devices
Recent clearances: LunaGuard Nighttime Dental Protector
1
Total
1
Cleared
0
Denied
Mckeon Products has 1 FDA 510(k) cleared medical devices. Based in Warren, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Mckeon Products Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Right Submission, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mckeon Products
1 devices