K243587
- 510(k) number
- K243587
- Device name
- PureLift GLOW
- Applicant
- Xtreem Pulse, LLC NY · US
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2025-03-06
- Date received
- 2024-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K243587.pdf
Official FDA record: K243587
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.