FDA Product Code
FDA Product Code GXW — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.1240
510(k) Clearances — 7 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K921863 | SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS | Hewlett-Packard Co. | 1992-09-28 | Traditional | PDF ↗ |
| K903085 | SMS-712NA | Toshiba America Medical Systems, In.C | 1990-10-05 | Traditional | PDF ↗ |
| K853432 | 5.0 IOP & 7.5 IOP PROBES | Diasonics, Inc. | 1986-02-07 | Traditional | PDF ↗ |
| K833522 | NEURO SECTOR FIXATION DEVICE | Advanced Technology Laboratories, Inc. | 1984-05-25 | Traditional | PDF ↗ |
| K821736 | ECHO-PULSE KM555 | Rabar, Inc. | 1982-12-09 | Traditional | PDF ↗ |
| K770788 | ECHOENCEPHALOGRAPH, DIGITAL,DIGIECHO2000 | Storz Instrument Co. | 1977-05-06 | Traditional | PDF ↗ |
| K770575 | ECHOENCEPHALOGRAPH, DIGITAL, 1000 | Storz Instrument Co. | 1977-04-26 | Traditional | PDF ↗ |
Product code GXW · Class II · Neurology. Data: openFDA.