The following data is part of a premarket notification filed by A-dec, Inc. with the FDA for A-dec 1040 Chair.
| Device ID | K925119 |
| 510k Number | K925119 |
| Device Name: | A-DEC 1040 CHAIR |
| Classification | Chair, Dental, With Operative Unit |
| Applicant | A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
| Contact | Tony Tewell |
| Correspondent | Tony Tewell A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
| Product Code | KLC |
| CFR Regulation Number | 872.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-09 |
| Decision Date | 1994-01-31 |