The following data is part of a premarket notification filed by Tri W-g, Inc. with the FDA for Treatment Table.
| Device ID | K910838 |
| 510k Number | K910838 |
| Device Name: | TREATMENT TABLE |
| Classification | Table, Radiographic, Tilting |
| Applicant | TRI W-G, INC. P.O. BOX 905 Valley City, ND 58072 |
| Contact | David Kesler |
| Correspondent | David Kesler TRI W-G, INC. P.O. BOX 905 Valley City, ND 58072 |
| Product Code | IXR |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-02-27 |
| Decision Date | 1991-08-07 |