The following data is part of a premarket notification filed by Hypoguard Usa, Inc. with the FDA for Hypoguard Advance Blood Glucose Monitoring System.
| Device ID | K020232 |
| 510k Number | K020232 |
| Device Name: | HYPOGUARD ADVANCE BLOOD GLUCOSE MONITORING SYSTEM |
| Classification | Glucose Oxidase, Glucose |
| Applicant | HYPOGUARD USA, INC. 5182 WEST 76TH ST. Edina, MN 55439 |
| Contact | Bruce A Macfarlane |
| Correspondent | Bruce A Macfarlane HYPOGUARD USA, INC. 5182 WEST 76TH ST. Edina, MN 55439 |
| Product Code | CGA |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-01-14 |
| Decision Date | 2002-02-12 |
| Summary: | summary |