Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507)

FDA 510(k) K251662 · Shenzhen Future Electronic Co., Ltd.

Substantially Equivalent

510(k) numberK251662

Submission

Device name
Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507)
Applicant
Shenzhen Future Electronic Co., Ltd.
Shenzhen, CN
Received
May 30, 2025
Decision date
November 13, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IRP – Massager, Powered Inflatable Tube
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5650
Specialty
Physical Medicine

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K253064Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air…IRP · Traditional Xiamen Weiyou Intelligent Technology Co., Ltd.04/30/2026SE
K252386Hot and Cold Compression System (A02-C-032)IRP · Traditional Chengdu Cryo-Push Medical Technology Co.,Ltd04/03/2026SE
K253076Cryopush Cold Compression Device (A02-P-001)IRP · Traditional Chengdu Cryo-Push Medical Technology Co.,Ltd04/02/2026SE
K251622Hand Massager (SM004D)IRP · Traditional Ningbo Zhenhai Yihao Electronic Technology Co.…01/28/2026SE

More from Ningbo Zhenhai Yihao Electronic Technology Co., Ltd.

510(k)DeviceDecision
K221092Transcutaneous Electrical Nerve Stimulator Model: ST-304NUH · Traditional 09/13/2022SE
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Questions and answers

When was Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507) cleared by the FDA?

Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507) (K251662) received a 510(k) decision of Substantially Equivalent on November 13, 2025, 167 days after the submission was received.

What is the product code of K251662?

The FDA product code is IRP – Massager, Powered Inflatable Tube, a Class II (moderate risk) device regulated under 21 CFR 890.5650.