Argus Photonics Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argus Photonics Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Argus Photonics Group has 2 FDA 510(k) cleared medical devices. Based in Jupiter, US.
Historical record: 2 cleared submissions from 1997 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Argus Photonics Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Argus Photonics Group
2 devices