K-number	K181660
Device name	Acapella Choice Blue Vibratory PEP Device
Applicant	Smiths Medical
Product code	BWF
Device class	Class II
Decision date	Oct 24, 2019
Decision	Substantially Equivalent
Regulation	868.5690

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Source

View the full FDA submission: accessdata.fda.gov

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Acapella Choice Blue Vibratory PEP Device

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