| Primary Device ID | GYNX9501 |
| NIH Device Record Key | 0da054c9-8c4e-4616-9eb3-9909546ef51f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Electrode Handpiece, Foot Activated |
| Version Model Number | 950 |
| Company DUNS | 012997685 |
| Company Name | GYNEX CORPORATION |
| Device Count | 12 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |