The following data is part of a premarket notification filed by Ivoclar Vivadent, Inc. with the FDA for Excite F And Excite Dsc.
| Device ID | K093744 |
| 510k Number | K093744 |
| Device Name: | EXCITE F AND EXCITE DSC |
| Classification | Agent, Tooth Bonding, Resin |
| Applicant | IVOCLAR VIVADENT, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Donna Marie Hartnett |
| Correspondent | Donna Marie Hartnett IVOCLAR VIVADENT, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | KLE |
| CFR Regulation Number | 872.3200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-12-04 |
| Decision Date | 2010-03-10 |
| Summary: | summary |