The following data is part of a premarket notification filed by Orbusneich Medical (shenzhen) Co., Ltd. with the FDA for Sapphire Nc 24.
| Device ID | K211807 |
| 510k Number | K211807 |
| Device Name: | Sapphire NC 24 |
| Classification | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
| Applicant | OrbusNeich Medical (Shenzhen) Co., Ltd. No.1 Jinkui Road, Futian Free Trade Zone Shenzhen, CN 518038 |
| Contact | Daniel Zhang |
| Correspondent | Daniel Zhang OrbusNeich Medical (Shenzhen) Co., Ltd. No.1 Jinkui Road, Futian Free Trade Zone Shenzhen, CN 518038 |
| Product Code | LOX |
| CFR Regulation Number | 870.5100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-06-11 |
| Decision Date | 2021-10-14 |