The following data is part of a premarket notification filed by Pulpdent Corporation with the FDA for Lime-lite Ii.
| Device ID | K113711 |
| 510k Number | K113711 |
| Device Name: | LIME-LITE II |
| Classification | Liner, Cavity, Calcium Hydroxide |
| Applicant | PULPDENT CORPORATION 80 Oakland St Watertown, MA 02472 |
| Contact | Kenneth J Berk |
| Correspondent | Kenneth J Berk PULPDENT CORPORATION 80 Oakland St Watertown, MA 02472 |
| Product Code | EJK |
| CFR Regulation Number | 872.3250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-12-19 |
| Decision Date | 2012-03-05 |
| Summary: | summary |