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 |