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FDA 510(k)

FINESUN EMS STIMULATOR

K-Number: K020684 · 2002-05-23

ApplicantFinesun Worldwide Intl. Co., Ltd.
Decision Date2002-05-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FINESUN EMS STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Finesun Worldwide Intl. Co., Ltd.. It received FDA 510(k) clearance on 2002-05-23 under 510(k) number K020684. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINESUN EMS STIMULATOR?

FINESUN EMS STIMULATOR is a medical device that received FDA 510(k) clearance on 2002-05-23. The listed applicant is Finesun Worldwide Intl. Co., Ltd.. The 510(k) number is K020684.

When did FINESUN EMS STIMULATOR receive FDA 510(k) clearance?

FINESUN EMS STIMULATOR received FDA 510(k) clearance on 2002-05-23, under 510(k) number K020684.

Who is the listed applicant for FINESUN EMS STIMULATOR?

The FDA 510(k) record lists Finesun Worldwide Intl. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FINESUN EMS STIMULATOR?

The FDA product code for FINESUN EMS STIMULATOR is IPF.

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Related Devices (Code: IPF)

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Official Source

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

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