Algomedica is one of 18524 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Algomedica has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Algomedica Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Devine Guidance International, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Algomedica
1 devices