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FDA 510(k)

Intrelief

K-Number: K211263 · 2021-12-30

ApplicantEasymed Instruments Co., Ltd.
Decision Date2021-12-30
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Intrelief is a medical device manufactured by Easymed Instruments Co., Ltd.. It received FDA 510(k) clearance on 2021-12-30 under approval number K211263. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intrelief?

Intrelief is a medical device that received FDA 510(k) clearance on 2021-12-30. It is manufactured by Easymed Instruments Co., Ltd.. The 510(k) number is K211263.

When was Intrelief approved by the FDA?

Intrelief received FDA 510(k) clearance on 2021-12-30, under approval number K211263.

What company makes Intrelief?

Intrelief is manufactured by Easymed Instruments Co., Ltd..

What is the FDA product code for Intrelief?

The FDA product code for Intrelief is NUH.

Other Devices by Easymed Instruments Co., Ltd.

K241899Pelvic Floor Stimulator (Intrelief PFE)

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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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