Roche Diagnostics Corp.
201 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| PO2 electrode for Roche AVL OMNI Analyzers. Catalog number BP1734. recall (Z-0438-03) | Roche Diagnostics Corp. | 2003-01-23 |
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Every clearance here is in the API, with alerts when new ones post.