K-number	K181110
Device name	PROPHYflex 4
Applicant	Kaltenbach & Voigt GmbH
Product code	EFB
Device class	Class I
Decision date	Apr 10, 2019
Decision	Substantially Equivalent
Regulation	872.4200

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Source

View the full FDA submission: accessdata.fda.gov

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PROPHYflex 4

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