Ark Diagnostics, Inc. · Class II · Cleared Apr 16, 2009
| K-number | K083799 |
| Device name | TOPIRAMATE ASSAY, ARK TOPIRAMATE CALIBRATOR AND ARK TOPIRAMATE CONTROL, MODELS 5015-0001-000, 5015-0002-00, 5015-0003-00 |
| Applicant | Ark Diagnostics, Inc. |
| Product code | NWM |
| Device class | Class II |
| Decision date | Apr 16, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 862.3350 |
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