K-number	K220114
Device name	PowerPAK Syringe
Applicant	Vault Paragon Group, Inc.
Product code	MEG
Device class	Class II
Decision date	Jan 25, 2023
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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PowerPAK Syringe

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