510(k) K251662

Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507) by Shenzhen Future Electronic Co., Ltd. — Product Code IRP

K251662 is an FDA 510(k) premarket notification submitted by Shenzhen Future Electronic Co., Ltd. for the device "Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507)". The FDA issued a decision of Substantially Equivalent on November 13, 2025. The device falls under product code IRP (Massager, Powered Inflatable Tube), a Class II device regulated under 21 CFR 890.5650. Shenzhen Future Electronic Co., Ltd. has at least 2 other 510(k) clearances on record.