K-number	K230813
Device name	BlueStar and BlueStar Rx
Applicant	Welldoc, Inc.
Product code	NDC
Device class	Class II
Decision date	Jul 28, 2023
Decision	Substantially Equivalent
Regulation	868.1890

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Source

View the full FDA submission: accessdata.fda.gov

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BlueStar and BlueStar Rx

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