Automated Screening Devices
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| SENTRY (K792653) | Automated Screening Devices | 1980-01-04 |
| MONITOR, NON-INVASIVE BLOOD PRESSURE (K782000) | Automated Screening Devices | 1978-12-05 |
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