Class Class II

AvalancheLase Family (K223540)

K223540 2023-01-19 Traditional
Home/ Devices/ AvalancheLase Family (K223540)

Description

AvalancheLase Family by Fotona D.O.O. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223540
Clearance Date2023-01-19
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top