The following data is part of a premarket notification filed by Tri W-g, Inc. with the FDA for Table, Models 610,611 & 612.
| Device ID | K834103 |
| 510k Number | K834103 |
| Device Name: | TABLE, MODELS 610,611 & 612 |
| Classification | Table, Powered |
| Applicant | TRI W-G, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-29 |
| Decision Date | 1984-01-13 |