The following data is part of a premarket notification filed by Parkell, Inc. with the FDA for Hyperfil-lv.
Device ID | K182296 |
510k Number | K182296 |
Device Name: | HyperFil-LV |
Classification | Material, Tooth Shade, Resin |
Applicant | Parkell, Inc. 300 Executive Drive Edgewood, NY 11717 |
Contact | David Mott |
Correspondent | David Mott Parkell, Inc. 300 Executive Drive Edgewood, NY 11717 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-24 |
Decision Date | 2018-12-14 |
Summary: | summary |