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FDA 510(k)

Air compression leg massager HY-1117A

K-Number: K212713 · 2022-01-18

Decision Date2022-01-18
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air compression leg massager HY-1117A is a medical device manufactured by Xiamen High Top Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-01-18 under approval number K212713. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Air compression leg massager HY-1117A?

Air compression leg massager HY-1117A is a medical device that received FDA 510(k) clearance on 2022-01-18. It is manufactured by Xiamen High Top Electronic Technology Co., Ltd.. The 510(k) number is K212713.

When was Air compression leg massager HY-1117A approved by the FDA?

Air compression leg massager HY-1117A received FDA 510(k) clearance on 2022-01-18, under approval number K212713.

What company makes Air compression leg massager HY-1117A?

Air compression leg massager HY-1117A is manufactured by Xiamen High Top Electronic Technology Co., Ltd..

What is the FDA product code for Air compression leg massager HY-1117A?

The FDA product code for Air compression leg massager HY-1117A is IRP.

Related Devices (Code: IRP)

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.