K232567
- 510(k) number
- K232567
- Device name
- Myriad SPECTRA Light Source
- Applicant
- Nico Corporation IN · US
- Product code
- QFX — Diagnostic Neurosurgical Microscope Filter
- Decision date
- 2024-03-14
- Date received
- 2023-08-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K232567.pdf
Official FDA record: K232567
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.