Class Class II

Single Use Bipolar Forceps (K230432)

K230432 2023-05-18 Traditional
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Description

Single Use Bipolar Forceps by Hg Innovations, Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230432
Clearance Date2023-05-18
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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