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FDA 510(k)

Endo Motor

K-Number: K203320 · 2021-05-10

ApplicantGuilin Woodpecker Medical Instrument Co., Ltd.
Decision Date2021-05-10
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Endo Motor is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2021-05-10 under approval number K203320. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endo Motor?

Endo Motor is a medical device that received FDA 510(k) clearance on 2021-05-10. It is manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K203320.

When was Endo Motor approved by the FDA?

Endo Motor received FDA 510(k) clearance on 2021-05-10, under approval number K203320.

What company makes Endo Motor?

Endo Motor is manufactured by Guilin Woodpecker Medical Instrument Co., Ltd..

What is the FDA product code for Endo Motor?

The FDA product code for Endo Motor is EKX.

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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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