Class Class II

Safety Lancet (K222801)

K222801 2023-01-25 Traditional
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Description

Safety Lancet by Sarstedt AG & CO KG — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222801
Clearance Date2023-01-25
Clearance TypeTraditional
Product CodeFMK
Regulation Number878.4850

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