K-number	K200017
Device name	Eclipse DermaFlex Cannula
Applicant	Eclipse Medcorp, LLC
Product code	FMI
Device class	Class II
Decision date	Nov 5, 2020
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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Eclipse DermaFlex Cannula

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