Class Class II

E Blator (K251899)

K251899 2025-10-01 Traditional
Home/ Devices/ E Blator (K251899)

Description

E Blator by New Deantronics Taiwan , Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251899
Clearance Date2025-10-01
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top