Air Compression Leg Massager (K-705)
K-Number: K242140 · 2025-03-17
Decision Date2025-03-17
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Air Compression Leg Massager (K-705) is a medical device manufactured by Jiale Health Technology Shenzhen Co., Ltd.. It received FDA 510(k) clearance on 2025-03-17 under approval number K242140. 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 (K-705)?
Air Compression Leg Massager (K-705) is a medical device that received FDA 510(k) clearance on 2025-03-17. It is manufactured by Jiale Health Technology Shenzhen Co., Ltd.. The 510(k) number is K242140.
When was Air Compression Leg Massager (K-705) approved by the FDA?
Air Compression Leg Massager (K-705) received FDA 510(k) clearance on 2025-03-17, under approval number K242140.
What company makes Air Compression Leg Massager (K-705)?
Air Compression Leg Massager (K-705) is manufactured by Jiale Health Technology Shenzhen Co., Ltd..
What is the FDA product code for Air Compression Leg Massager (K-705)?
The FDA product code for Air Compression Leg Massager (K-705) 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.