Class Class II

Coolfase (K250852)

K250852 2025-10-16 Traditional
Home/ Devices/ Coolfase (K250852)

Description

Coolfase by Asterasys Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250852
Clearance Date2025-10-16
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