Class Class II

PowerPAK Syringe (K220114)

K220114 2023-01-25 Traditional
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Description

PowerPAK Syringe by Vault Paragon Group, Inc. — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220114
Clearance Date2023-01-25
Clearance TypeTraditional
Product CodeMEG
Regulation Number880.5860

Categories

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