Class Class II

Transit-Pellets (K222000)

K222000 2023-01-18 Traditional
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Description

Transit-Pellets by Medifactia AB — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222000
Clearance Date2023-01-18
Clearance TypeTraditional
Product CodeFFX
Regulation Number876.1725

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