GZK — Electrode, Nasopharyngeal Class II
FDA Device Classification
Classification Details
- Product Code
- GZK
- Device Class
- Class II
- Regulation Number
- 882.1340
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K030517 | viasys healthcare | BALL RECORDING ELECTRODE/STIMULATION PROBE | August 1, 2003 |
| K830325 | bertone and assoc | TIGER PULSE | March 1, 1983 |