K253261
- 510(k) number
- K253261
- Device name
- Apollo Quattro (APQ-10M)
- Applicant
- Weero Co., Ltd. KR
- Product code
- PBX — Massager, Vacuum, Radio Frequency Induced Heat
- Decision date
- 2026-03-13
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K253261.pdf
Official FDA record: K253261
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.