FDA Product Code
FDA Product Code GXX — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.1925
510(k) Clearances — 3 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K893216 | RMI ULTRASOUND DOPPLER PHANTOM SYSTEM | Radiation Measurements, Inc. | 1989-09-05 | Traditional | PDF ↗ |
| K844120 | ULTRASONIC SCANNER CALIBRATION & TEST OBJECTS | Echo Ultrasound | 1985-01-23 | Traditional | PDF ↗ |
| K844247 | ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMS | Technicare Corp. | 1985-01-23 | Traditional | PDF ↗ |
Product code GXX · Class I · Neurology. Data: openFDA.