Allelix Diagnostics, Inc.
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| VISUWELL REAGIN TEST 960 TEST KIT (K885298) | Allelix Diagnostics, Inc. | 1989-03-15 |
| MODIFIED GROUP A STREPTOCOCCUS DETECTION KIT (K880665) | Allelix Diagnostics, Inc. | 1988-03-01 |
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Every clearance here is in the API, with alerts when new ones post.