Quinton Electrophysiology Corp.
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391 (K971570) | Quinton Electrophysiology Corp. | 1997-12-29 |
| EP AMP, MODEL #901 (K925346) | Quinton Electrophysiology Corp. | 1993-04-30 |
| EPLAB (ELECTROCARDIOGRAPHIC MONITOR) (K893836) | Quinton Electrophysiology Corp. | 1989-09-08 |
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