Class Class II

Omnipod GO Insulin Delivery Device (K223372)

K223372 2023-04-24 Traditional
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Description

Omnipod GO Insulin Delivery Device by Insulet Corporation — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223372
Clearance Date2023-04-24
Clearance TypeTraditional
Product CodeLZG
Regulation Number880.5725

Categories

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