Class Class II

OmniGuide RFID Surgical Laser Fibers (K230819)

K230819 2023-04-21 Special
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Description

OmniGuide RFID Surgical Laser Fibers by Omni-Guide Holdings, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230819
Clearance Date2023-04-21
Clearance TypeSpecial
Product CodeGEX
Regulation Number878.4810

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