Applied Photonix, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Photonix, LLC - FDA 510(k) Cleared Devices
Recent clearances: ViroZap Indoor Air Purifier, In Duct Model 1008
1
Total
1
Cleared
0
Denied
Applied Photonix, LLC has 1 FDA 510(k) cleared medical devices. Based in Tampa, US.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Applied Photonix, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by King & Spalding Llp as regulatory consultant.
FDA 510(k) Regulatory Record - Applied Photonix, LLC
1 devices