The following data is part of a premarket notification filed by Foremost Dental Mfg., Inc. with the FDA for Zenith Luxacore Automix Core Material (multiple).
Device ID | K982201 |
510k Number | K982201 |
Device Name: | ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE) |
Classification | Material, Tooth Shade, Resin |
Applicant | FOREMOST DENTAL MFG., INC. 242 SOUTH DEAN ST. Englewood, NJ 07631 |
Contact | D T Wolf |
Correspondent | D T Wolf FOREMOST DENTAL MFG., INC. 242 SOUTH DEAN ST. Englewood, NJ 07631 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-06-22 |
Decision Date | 1998-08-10 |