The following data is part of a premarket notification filed by Applied Medical Resources Corp. with the FDA for Voyant Maryland Fusion Device.
| Device ID | K182653 |
| 510k Number | K182653 |
| Device Name: | Voyant Maryland Fusion Device |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | Applied Medical Resources Corp. 22872 Avenida Empresa Rancho Santa Margarita, CA 92688 |
| Contact | Andrew Nguyen |
| Correspondent | Andrew Nguyen Applied Medical Resources Corp. 22872 Avenida Empresa Rancho Santa Margarita, CA 92688 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-09-25 |
| Decision Date | 2018-11-14 |
| Summary: | summary |