FDA Product Code
FDA Product Code QFX — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.4950
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K254030 | cCeLL405 | VPIX Medical, Inc. | 2026-10-02 | Traditional | PDF ↗ |
| K251286 | Affirm 400 | Digital Surgery Systems, Inc. (D.B.A True Digital Surgery) | 2026-01-21 | Traditional | PDF ↗ |
| K240215 | BLUE 400; BLUE 400 S | Carl Zeiss Meditec, AG | 2024-06-28 | Traditional | PDF ↗ |
| K232567 | Myriad SPECTRA Light Source | Nico Corporation | 2024-03-14 | Traditional | PDF ↗ |
| K211346 | BLUE 400 | Carl Zeiss Meditec, AG | 2022-07-22 | Traditional | PDF ↗ |
| DEN180024 | Leica FL400 | Leica Microsystems (Schweiz) AG | 2019-03-28 | Direct | — |
Product code QFX · Class II · Neurology. Data: openFDA.