GXX
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Block, Test, Ultrasonic Scanner Calibration
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 882.1925
- Medical specialty
- Neurology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| RMI ULTRASOUND DOPPLER PHANTOM SYSTEM (K893216) | Radiation Measurements, Inc. | 1989-09-05 |
| ULTRASONIC SCANNER CALIBRATION & TEST OBJECTS (K844120) | Echo Ultrasound | 1985-01-23 |
| ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMS (K844247) | Technicare Corp. | 1985-01-23 |
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