K251662
- 510(k) number
- K251662
- 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. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2025-11-13
- Date received
- 2025-05-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K251662.pdf
Official FDA record: K251662
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.