Diagnostic Hybrids Inc
3 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| MicroVue Bb Plus EIA is packaged as a kit which contains all reagent components to perform recall (Z-0417-2015) | Diagnostic Hybrids Inc | 2015-09-03 |
| Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture recall (Z-0792-2013) | Diagnostic Hybrids Inc | 2013-02-07 |
| Rabbit Kidney Culture, brand name: 'FreshCells'. The product is labeled as 'Rabbit Kidney' recall (Z-0822-2010) | Diagnostic Hybrids Inc | 2010-02-24 |
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Every clearance here is in the API, with alerts when new ones post.