Air Compression Therapy Device, model: ST-502
K-Number: K213745 · 2022-03-31
ApplicantShenzhen Future Electronic Co., Ltd.
Decision Date2022-03-31
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Air Compression Therapy Device, model: ST-502 is a medical device manufactured by Shenzhen Future Electronic Co., Ltd.. It received FDA 510(k) clearance on 2022-03-31 under approval number K213745. 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 Therapy Device, model: ST-502?
Air Compression Therapy Device, model: ST-502 is a medical device that received FDA 510(k) clearance on 2022-03-31. It is manufactured by Shenzhen Future Electronic Co., Ltd.. The 510(k) number is K213745.
When was Air Compression Therapy Device, model: ST-502 approved by the FDA?
Air Compression Therapy Device, model: ST-502 received FDA 510(k) clearance on 2022-03-31, under approval number K213745.
What company makes Air Compression Therapy Device, model: ST-502?
Air Compression Therapy Device, model: ST-502 is manufactured by Shenzhen Future Electronic Co., Ltd..
What is the FDA product code for Air Compression Therapy Device, model: ST-502?
The FDA product code for Air Compression Therapy Device, model: ST-502 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.