The following data is part of a premarket notification filed by Fine Advanced Compound Co., Ltd with the FDA for Non-sterile Zirconia Block.
Device ID | K190112 |
510k Number | K190112 |
Device Name: | Non-Sterile Zirconia Block |
Classification | Powder, Porcelain |
Applicant | Fine Advanced Compound Co., Ltd 7, Galgot-gil, Jinwi-myeon Pyeongtaek, KR |
Contact | Jeong Kwang-ho |
Correspondent | Chris Park Med.com 1809 Holland Dr Somerset, NJ 08873 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-01-23 |
Decision Date | 2019-12-20 |