The following data is part of a premarket notification filed by Home Diagnostics, Inc. with the FDA for Modification To Truetrack Smart System Blood Glucose Meter, Test Strips And Glucose Control.
| Device ID | K040670 |
| 510k Number | K040670 |
| Device Name: | MODIFICATION TO TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER, TEST STRIPS AND GLUCOSE CONTROL |
| Classification | System, Test, Blood Glucose, Over The Counter |
| Applicant | HOME DIAGNOSTICS, INC. 2400 N.W. 55TH CT. Fort Lauderdale, FL 33309 |
| Contact | Karen Devincent |
| Correspondent | Karen Devincent HOME DIAGNOSTICS, INC. 2400 N.W. 55TH CT. Fort Lauderdale, FL 33309 |
| Product Code | NBW |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-03-15 |
| Decision Date | 2004-03-25 |