The following data is part of a premarket notification filed by A-dec, Inc. with the FDA for A-dec 2183 Duo Unit, Cusp.
| Device ID | K925323 |
| 510k Number | K925323 |
| Device Name: | A-DEC 2183 DUO UNIT, CUSP |
| Classification | Chair, Dental, With Operative Unit |
| Applicant | A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
| Contact | Pat Ridenour |
| Correspondent | Pat Ridenour 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 | 1992-10-21 |
| Decision Date | 1993-12-09 |