The following data is part of a premarket notification filed by Tri W-g, Inc. with the FDA for Tri W-g, Inc Table, Tilt/exam/treatment Model 777.
| Device ID | K960196 |
| 510k Number | K960196 |
| Device Name: | TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 |
| Classification | Table, Powered |
| Applicant | TRI W-G, INC. 215 12TH AVE., N.E. P.O. BOX 905 Valley City, ND 58072 |
| Contact | David Kesler |
| Correspondent | David Kesler TRI W-G, INC. 215 12TH AVE., N.E. P.O. BOX 905 Valley City, ND 58072 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-16 |
| Decision Date | 1996-02-07 |