The following data is part of a premarket notification filed by Agamatrix with the FDA for Jazz Blood Glucose Monitoring System.
Device ID | K071393 |
510k Number | K071393 |
Device Name: | 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 |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-05-21 |
Decision Date | 2007-07-20 |
Summary: | summary |