The following data is part of a premarket notification filed by Contraves Goerz Corp. with the FDA for Computerized Posture Platform.
| Device ID | K771618 |
| 510k Number | K771618 |
| Device Name: | COMPUTERIZED POSTURE PLATFORM |
| Classification | Apparatus, Vestibular Analysis |
| Applicant | CONTRAVES GOERZ CORP. 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 | 1977-08-24 |
| Decision Date | 1977-09-12 |