The following data is part of a premarket notification filed by Bionime Coporation with the FDA for Ge333 Blood Glucose Monitoring System.
| Device ID | K143387 |
| 510k Number | K143387 |
| Device Name: | GE333 Blood Glucose Monitoring System |
| Classification | System, Test, Blood Glucose, Over The Counter |
| Applicant | Bionime Coporation No. 100, Sec. 2, Daqing St., South Dist. Taichung, TW 40242 |
| Contact | Tino Lee |
| Correspondent | Feng-yu Lee IVDD Regulatory Consultant 29222 Rancho Viejo Road, Suite 218 San Juan Capistrano, CA 92675 |
| Product Code | NBW |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-11-26 |
| Decision Date | 2015-06-03 |
| Summary: | summary |