FDA Product Code
FDA Product Code GZK — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.1340
510(k) Clearances — 2 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K030517 | BALL RECORDING ELECTRODE/STIMULATION PROBE | Viasys Healthcare, Inc. | 2003-08-01 | Abbreviated | PDF ↗ |
| K830325 | TIGER PULSE | Bertone & Assoc. | 1983-03-01 | Traditional | PDF ↗ |
Product code GZK · Class II · Neurology. Data: openFDA.