Class Class II

SurBlate Ablation System (K223272)

K223272 2023-02-28 Traditional
Home/ Devices/ SurBlate Ablation System (K223272)

Description

SurBlate Ablation System by Mima-Pro Scientific, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223272
Clearance Date2023-02-28
Clearance TypeTraditional
Product CodeNEY
Regulation Number878.4400

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