Class Class II

TRACHEOBRONXANE™ DUMON® (K243126)

K243126 2024-10-29 Special
Home/ Devices/ TRACHEOBRONXANE™ DUMON® (K243126)

Description

TRACHEOBRONXANE™ DUMON® by Novatech SA, an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243126
Clearance Date2024-10-29
Clearance TypeSpecial
Product CodeNWA
Regulation Number878.3720

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top