The following data is part of a premarket notification filed by Cavex Holland B.v. with the FDA for Quadrant Core Lc.
Device ID | K984042 |
510k Number | K984042 |
Device Name: | QUADRANT CORE LC |
Classification | Material, Tooth Shade, Resin |
Applicant | CAVEX HOLLAND B.V. 2003 RW HAARLEM PO BOX 852 Harmen, NL 19-21 |
Contact | Bernard Van Duijn |
Correspondent | Bernard Van Duijn CAVEX HOLLAND B.V. 2003 RW HAARLEM PO BOX 852 Harmen, NL 19-21 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-11-13 |
Decision Date | 1998-12-04 |