Echoencephalograph
FDA product code GXW · Class II (moderate risk) · 21 CFR 882.1240 · Neurology
7510(k) clearances
0PMA approvals
0recalls
Manufacturers
510(k) clearances
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K921863 | Sonos 500, 1000, 1500/SONOS or Ultrasound Imag SysGXW · Traditional | Hewlett-Packard Co. | 09/28/1992SE |
| K903085 | SMS-712NAGXW · Traditional | Toshiba America Medical Systems, In.C | 10/05/1990SE |
| K853432 | 5.0 Iop & 7.5 Iop ProbesGXW · Traditional | Diasonics, Inc. | 02/07/1986SE |
| K833522 | Neuro Sector Fixation DeviceGXW · Traditional | Advanced Technology Laboratories, Inc. | 05/25/1984SE |
| K821736 | Echo-Pulse KM555GXW · Traditional | Rabar, Inc. | 12/09/1982SE |
| K770788 | Echoencephalograph, DIGITAL,DIGIECHO2000GXW · Traditional | Storz Instrument Co. | 05/06/1977SE |
| K770575 | Echoencephalograph, Digital, 1000GXW · Traditional | Storz Instrument Co. | 04/26/1977SE |