Skip to content
Scan

Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K223540

AvalancheLase Family · Fotona D.O.O. · decided 2023-01-19 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
AvalancheLaseM071-2F/LXPFOTONA d.o.o.GEX03830054230361
AvalancheLaseM071-2F/LXFOTONA d.o.o.GEX03830054230378
AvalancheLaseM071-2F/XPFOTONA d.o.o.GEX03830054230385