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FDA 510(k)

KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138

K-Number: K062453 · 2007-04-17

ApplicantKingly Star Intl. Technology Co., Ltd.
Decision Date2007-04-17
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138 is the device name listed in this FDA 510(k) record. The listed applicant is Kingly Star Intl. Technology Co., Ltd.. It received FDA 510(k) clearance on 2007-04-17 under 510(k) number K062453. 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 KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138?

KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138 is a medical device that received FDA 510(k) clearance on 2007-04-17. The listed applicant is Kingly Star Intl. Technology Co., Ltd.. The 510(k) number is K062453.

When did KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138 receive FDA 510(k) clearance?

KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138 received FDA 510(k) clearance on 2007-04-17, under 510(k) number K062453.

Who is the listed applicant for KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138?

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

What is the FDA product code for KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138?

The FDA product code for KINGLY STAR POWERED MUSCLE STIMULATOR, MODEL KS-138 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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