Class Class II

LIGHTSCALPEL LS-4020 (K213669)

K213669 2023-02-15 Traditional
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Description

LIGHTSCALPEL LS-4020 by Lightscalpel, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213669
Clearance Date2023-02-15
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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