Dizzydoctor Systems, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dizzydoctor Systems, LLC - FDA 510(k) Cleared Devices
Recent clearances: DizzyDoctor System 1.0.0
1
Total
1
Cleared
0
Denied
Dizzydoctor Systems, LLC has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Dizzydoctor Systems, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dizzydoctor Systems, LLC
1 devices