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FDA 510(k)

JI-EE ELECTRIC SCOOTER, ESTHETE ES 1

K-Number: K024325 · 2003-04-04

Decision Date2003-04-04
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JI-EE ELECTRIC SCOOTER, ESTHETE ES 1 is the device name listed in this FDA 510(k) record. The listed applicant is Ji-Ee Industry Co., Ltd.. It received FDA 510(k) clearance on 2003-04-04 under 510(k) number K024325. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JI-EE ELECTRIC SCOOTER, ESTHETE ES 1?

JI-EE ELECTRIC SCOOTER, ESTHETE ES 1 is a medical device that received FDA 510(k) clearance on 2003-04-04. The listed applicant is Ji-Ee Industry Co., Ltd.. The 510(k) number is K024325.

When did JI-EE ELECTRIC SCOOTER, ESTHETE ES 1 receive FDA 510(k) clearance?

JI-EE ELECTRIC SCOOTER, ESTHETE ES 1 received FDA 510(k) clearance on 2003-04-04, under 510(k) number K024325.

Who is the listed applicant for JI-EE ELECTRIC SCOOTER, ESTHETE ES 1?

The FDA 510(k) record lists Ji-Ee Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JI-EE ELECTRIC SCOOTER, ESTHETE ES 1?

The FDA product code for JI-EE ELECTRIC SCOOTER, ESTHETE ES 1 is INI.

Related Clinical Trials

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.

Other records listing Ji-Ee Industry Co., Ltd. as applicant

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.

Related Devices (Code: INI)

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.

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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