Medtronic Versaflex, Inc.
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| MODELS 6526,6527,6528 PERCU. TRANS. ANGIO. CATH. (K891611) | Medtronic Versaflex, Inc. | 1989-06-12 |
| MODEL 611101 CONTRAST INJECTION DEVICE (K890898) | Medtronic Versaflex, Inc. | 1989-04-12 |
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