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FDA 510(k)

Feminine Personal Trainer (FPT)

K-Number: K171896 · 2017-08-29

ApplicantRalston Group
Decision Date2017-08-29
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Feminine Personal Trainer (FPT) is the device name listed in this FDA 510(k) record. The listed applicant is Ralston Group. It received FDA 510(k) clearance on 2017-08-29 under 510(k) number K171896. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Feminine Personal Trainer (FPT)?

Feminine Personal Trainer (FPT) is a medical device that received FDA 510(k) clearance on 2017-08-29. The listed applicant is Ralston Group. The 510(k) number is K171896.

When did Feminine Personal Trainer (FPT) receive FDA 510(k) clearance?

Feminine Personal Trainer (FPT) received FDA 510(k) clearance on 2017-08-29, under 510(k) number K171896.

Who is the listed applicant for Feminine Personal Trainer (FPT)?

The FDA 510(k) record lists Ralston Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Feminine Personal Trainer (FPT)?

The FDA product code for Feminine Personal Trainer (FPT) is HIR.

Related Devices (Code: HIR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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