510(k) K262419 ยท HCG Device, Neurovascular Embolization
MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730);
| Applicant | Cerenovus, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 14, 2026 |
| Received | Jul 15, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262419
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.