The following data is part of a premarket notification filed by Ok Biotech Co., Ltd. with the FDA for Prodigy Autocode Eject Blood Glucose Monitoring System.
| Device ID | K141914 |
| 510k Number | K141914 |
| Device Name: | PRODIGY AUTOCODE EJECT BLOOD GLUCOSE MONITORING SYSTEM |
| Classification | System, Test, Blood Glucose, Over The Counter |
| Applicant | OK BIOTECH CO., LTD. NO. 91, SEC. 2 GONGDAOWU 5TH ROAD Hsinchu City, TW 30070 |
| Contact | Ke-min Jen |
| Correspondent | Ke-min Jen OK BIOTECH CO., LTD. NO. 91, SEC. 2 GONGDAOWU 5TH ROAD Hsinchu City, TW 30070 |
| Product Code | NBW |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-07-15 |
| Decision Date | 2015-04-15 |
| Summary: | summary |