K253542
- 510(k) number
- K253542
- Device name
- Apollo Quattro (APQ-10M)
- Applicant
- Weero Co., Ltd. KR
- Product code
- IPF — Stimulator, Muscle, Powered
- Decision date
- 2026-06-08
- Date received
- 2025-11-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K253542.pdf
Official FDA record: K253542
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.