Squibb Diagnostics
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR (K883609) | Squibb Diagnostics | 1989-04-14 |
| RADIONUCLIDE INFUSION SYSTEM (K842568) | Squibb Diagnostics | 1984-10-19 |
| BICEPS ELECTROCAUTERY SYSTEM (K823755) | Squibb Diagnostics | 1983-01-26 |
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Every clearance here is in the API, with alerts when new ones post.