Hypoguard USA, Inc. · Class II · Cleared Mar 28, 2006
| K-number | K053079 |
| Device name | ASSURE PRO BLOOD GLUCOSE MONITORING SYSTEM, MODEL 460001 |
| Applicant | Hypoguard USA, Inc. |
| Product code | CGA |
| Device class | Class II |
| Decision date | Mar 28, 2006 |
| Decision | Substantially Equivalent |
| Regulation | 862.1345 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov