The following data is part of a premarket notification filed by Teca, Inc. with the FDA for Teca Vs6 Video Stimulator.
| Device ID | K781398 |
| 510k Number | K781398 |
| Device Name: | TECA VS6 VIDEO STIMULATOR |
| Classification | Stimulator, Photic, Evoked Response |
| Applicant | TECA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GWE |
| CFR Regulation Number | 882.1890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-08-15 |
| Decision Date | 1978-08-23 |