Air Compression Massager (Model LF-FT003)
K-Number: K213000 · 2021-11-15
Decision Date2021-11-15
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Air Compression Massager (Model LF-FT003) is a medical device manufactured by Wenzhou Lingfeng Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-11-15 under approval number K213000. 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 Massager (Model LF-FT003)?
Air Compression Massager (Model LF-FT003) is a medical device that received FDA 510(k) clearance on 2021-11-15. It is manufactured by Wenzhou Lingfeng Electronic Technology Co., Ltd.. The 510(k) number is K213000.
When was Air Compression Massager (Model LF-FT003) approved by the FDA?
Air Compression Massager (Model LF-FT003) received FDA 510(k) clearance on 2021-11-15, under approval number K213000.
What company makes Air Compression Massager (Model LF-FT003)?
Air Compression Massager (Model LF-FT003) is manufactured by Wenzhou Lingfeng Electronic Technology Co., Ltd..
What is the FDA product code for Air Compression Massager (Model LF-FT003)?
The FDA product code for Air Compression Massager (Model LF-FT003) 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.