Air Compression Leg Massager (model: FE-7204B)
K-Number: K211850 · 2022-03-03
ApplicantXiamen Healthpal Electronic Co.,Ltd
Decision Date2022-03-03
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Air Compression Leg Massager (model: FE-7204B) is a medical device manufactured by Xiamen Healthpal Electronic Co.,Ltd. It received FDA 510(k) clearance on 2022-03-03 under approval number K211850. 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 (model: FE-7204B)?
Air Compression Leg Massager (model: FE-7204B) is a medical device that received FDA 510(k) clearance on 2022-03-03. It is manufactured by Xiamen Healthpal Electronic Co.,Ltd. The 510(k) number is K211850.
When was Air Compression Leg Massager (model: FE-7204B) approved by the FDA?
Air Compression Leg Massager (model: FE-7204B) received FDA 510(k) clearance on 2022-03-03, under approval number K211850.
What company makes Air Compression Leg Massager (model: FE-7204B)?
Air Compression Leg Massager (model: FE-7204B) is manufactured by Xiamen Healthpal Electronic Co.,Ltd.
What is the FDA product code for Air Compression Leg Massager (model: FE-7204B)?
The FDA product code for Air Compression Leg Massager (model: FE-7204B) is IRP.
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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.