FDA 510(k), K171896, Feminine Personal Trainer (FPT)

FDA 510(k), K171896, Feminine Personal Trainer (FPT)

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510(K) Number: K171896
Device Name: Feminine Personal Trainer (FPT)
Manufacturer: Russell Ralston
Device Classification Name: Perineometer
Regulation Number: HIR
Classification Product Code: 06/26/2017
Date Received: 08/29/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology

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