The following data is part of a premarket notification filed by Henley Intl. with the FDA for Neurological Diagnostic Devices.
| Device ID | K943449 |
| 510k Number | K943449 |
| Device Name: | NEUROLOGICAL DIAGNOSTIC DEVICES |
| Classification | Electrode, Cutaneous |
| Applicant | HENLEY INTL. 104 INDUSTRIAL BLVD., Sugar Land, TX 77470 |
| Contact | Ernest J Henley |
| Correspondent | Ernest J Henley HENLEY INTL. 104 INDUSTRIAL BLVD., Sugar Land, TX 77470 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-07-18 |
| Decision Date | 1995-11-15 |