The following data is part of a premarket notification filed by Tri W-g, Inc. with the FDA for Autorange Model 205.
| Device ID | K822031 |
| 510k Number | K822031 |
| Device Name: | AUTORANGE MODEL 205 |
| Classification | Exerciser, Powered |
| Applicant | TRI W-G, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BXB |
| CFR Regulation Number | 890.5380 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-07-12 |
| Decision Date | 1982-07-26 |