The following data is part of a premarket notification filed by Diadent Group International with the FDA for Diafil Flow.
Device ID | K192284 |
510k Number | K192284 |
Device Name: | DiaFil Flow |
Classification | Material, Tooth Shade, Resin |
Applicant | Diadent Group International 16, Osongsaengmyeong 4-ro, Osong-eup, Heungdeok-gu Cheongji-si, KR 28161 |
Contact | Kab Sun Lee |
Correspondent | Kab Sun Lee Diadent Group International 16, Osongsaengmyeong 4-ro, Osong-eup, Heungdeok-gu Cheongji-si, KR 28161 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-08-22 |
Decision Date | 2020-03-25 |