Air Compression Therapy Device, model: ST-502
K-Number: K213745 · 2022-03-31
Device Summary
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. The listed applicant is Shenzhen Future Electronic Co., Ltd.. The 510(k) number is K213745.
When did Air Compression Therapy Device, model: ST-502 receive FDA 510(k) clearance?
Air Compression Therapy Device, model: ST-502 received FDA 510(k) clearance on 2022-03-31, under 510(k) number K213745.
Who is the listed applicant for Air Compression Therapy Device, model: ST-502?
The FDA 510(k) record lists Shenzhen Future Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Shenzhen Future Electronic Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IRP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.