Class Class II

Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator) (K252412)

K252412 2025-10-31 Traditional
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Description

Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator) by Applied Medical Resources Corporation, an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252412
Clearance Date2025-10-31
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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