The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for D-sense.
| Device ID | K955279 |
| 510k Number | K955279 |
| Device Name: | D-SENSE |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | CENTRIX, INC. 770 RIVER RD. Shelton, CT 06484 -5458 |
| Contact | John Discko |
| Correspondent | John Discko CENTRIX, INC. 770 RIVER RD. Shelton, CT 06484 -5458 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-16 |
| Decision Date | 1995-12-28 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817051020747 | K955279 | 000 |