Allelix, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K871620 | ALLELIX GROUP A STREPTOCOCCUS DETECTION KIT | GTZ | 1987-06-17 | View |
| 510(k) | K871308 | ALLELIX PREGNANCY DETECTION KIT 48 TEST KIT | JHI | 1987-06-11 | View |
No matching devices.
Advertisement