The following data is part of a premarket notification filed by Agamatrix with the FDA for Modification To: Jazz Blood Glucose Monitoring System.
| Device ID | K072413 |
| 510k Number | K072413 |
| Device Name: | MODIFICATION TO: JAZZ BLOOD GLUCOSE MONITORING SYSTEM |
| Classification | System, Test, Blood Glucose, Over The Counter |
| Applicant | AGAMATRIX 10 MAOR PARKWAY Salem, NH 03079 |
| Contact | Connie Hertel |
| Correspondent | Connie Hertel AGAMATRIX 10 MAOR PARKWAY Salem, NH 03079 |
| Product Code | NBW |
| Subsequent Product Code | CGA |
| Subsequent Product Code | JJX |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-28 |
| Decision Date | 2007-09-27 |
| Summary: | summary |