Binax, Inc. · Class I · Cleared Sep 4, 2009
| K-number | K091489 |
| Device name | CLEARVIEW ADVANCED STREP A , MODEL 737-430 |
| Applicant | Binax, Inc. |
| Product code | GTY |
| Device class | Class I |
| Decision date | Sep 4, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 866.3740 |
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