Class Class II

Resolv Endoscopic Hemostat System (K234131)

K234131 2024-07-26 Traditional
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Description

Resolv Endoscopic Hemostat System by Hemostasis, LLC — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK234131
Clearance Date2024-07-26
Clearance TypeTraditional
Product CodeQAU
Regulation Number878.4456

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