OQQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Diagnostic Ultrasonic Transducer, Robotic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.1570
- Medical specialty
- Radiology
- Flags
- Third-party review eligible
- FDA definition
- Diagnostic ultrasonic imaging or monitoring.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| TRANSCRANIAL AND VASCULAR DOPPLER DIAGNOTIC ULTRASOUND TRANSDUCERS, MODEL EMS-9UA (K092164) | Shenzhen Delicate Electronics Co., Ltd. | 2010-05-13 | + Add |
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