The following data is part of a premarket notification filed by Contraves with the FDA for Chair, Vestibular, Rotary, Comput..
| Device ID | K781268 |
| 510k Number | K781268 |
| Device Name: | CHAIR, VESTIBULAR, ROTARY, COMPUT. |
| Classification | Apparatus, Vestibular Analysis |
| Applicant | CONTRAVES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LXV |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-07-24 |
| Decision Date | 1978-08-14 |