The following data is part of a premarket notification filed by Mauna Kea Technologies with the FDA for Cellvizio 100 Series Systems With Confocal Miniprobes.
| Device ID | K180270 |
| 510k Number | K180270 |
| Device Name: | Cellvizio 100 Series Systems With Confocal Miniprobes |
| Classification | Endoscope, Neurological |
| Applicant | Mauna Kea Technologies 9 Rue D'Enghien Paris, FR 75010 |
| Contact | Veronique Dentan |
| Correspondent | Michael A. Daniel Daniel & Daniel Consulting 340 Jones Lane Gardnerville, NV 89460 |
| Product Code | GWG |
| CFR Regulation Number | 882.1480 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-01-31 |
| Decision Date | 2018-05-22 |
| Summary: | summary |