Class Class II

MOVIVA® Hybrid Ablation Probe (K253915)

K253915 2025-12-18 Traditional
Home/ Devices/ MOVIVA® Hybrid Ablation Probe…

Description

MOVIVA® Hybrid Ablation Probe by Erbe Elektromedizin GmbH, an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253915
Clearance Date2025-12-18
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