The following data is part of a premarket notification filed by Espe Dental Products with the FDA for Nimetic-dispers.
Device ID | K802049 |
510k Number | K802049 |
Device Name: | NIMETIC-DISPERS |
Classification | Material, Tooth Shade, Resin |
Applicant | ESPE DENTAL PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-08-25 |
Decision Date | 1980-09-16 |