K242441
- 510(k) number
- K242441
- Device name
- Revian Lyte (10011)
- Applicant
- Revian, Inc. NC · US
- Product code
- OAP — Laser, Comb, Hair
- Decision date
- 2024-09-13
- Date received
- 2024-08-16
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K242441.pdf
Official FDA record: K242441
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.