510(k) K232567 ยท QFX Diagnostic Neurosurgical Microscope Filter
Myriad SPECTRA Light Source
| Applicant | Nico Corporation, Indianapolis IN, US |
| Decision | Substantially Equivalent, Mar 14, 2024 |
| Received | Aug 24, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232567
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 26, 2025 | Stryker Corporation NICO Myriad Illumination Pack
Product No. NN-1000
11g Illumination Sleeve/Fiber;
Product No. NN-1001
13g Illumination Sleeve/Fiber Open, Classified |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.