K241931
- 510(k) number
- K241931
- Device name
- OcuMet Beacon (OCUB100)
- Applicant
- Ocusciences, Inc. MI · US
- Product code
- MYC — Ophthalmoscope, Laser, Scanning
- Decision date
- 2025-04-22
- Date received
- 2024-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K241931.pdf
Official FDA record: K241931
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.