Kdb Inc. (Dba) Sperti Sunlamp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kdb Inc. (Dba) Sperti Sunlamp - FDA 510(k) Cleared Devices
Recent clearances: FIJI SUN FLUORESCENT TANNING UNIT
1
Total
1
Cleared
0
Denied
Kdb Inc. (Dba) Sperti Sunlamp has 1 FDA 510(k) cleared medical devices. Based in Crescent Springs, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kdb Inc. (Dba) Sperti Sunlamp Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kdb Inc. (Dba) Sperti Sunlamp
1 devices