Air Compression Therapy Device (4 models)— 510(k) K251662

Name: FDA 510(k) clearance K251662
Creator: U.S. Food and Drug Administration
Published: 2025-11-13

Substantially Equivalent

Shenzhen Future Electronic Co., Ltd.

FDA 510(k) clearance K251662 for Air Compression Therapy Device (4 models), Substantially Equivalent on 2025-11-13. Applicant: Shenzhen Future Electronic Co., Ltd.. Device class: 2.

Clearance details

Device name as filed: 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.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2025-05-30
Decision date: 2025-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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