The following data is part of a premarket notification filed by A-dec, Inc. with the FDA for A-dec 200 Dental System.
| Device ID | K102234 |
| 510k Number | K102234 |
| Device Name: | A-DEC 200 DENTAL SYSTEM |
| Classification | Unit, Operative Dental |
| Applicant | A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
| Contact | Thomas H Louisell |
| Correspondent | Thomas H Louisell A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
| Product Code | EIA |
| CFR Regulation Number | 872.6640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-08-09 |
| Decision Date | 2010-11-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10194665003661 | K102234 | 000 |
| 10194665003630 | K102234 | 000 |