The following data is part of a premarket notification filed by U&c International Co., Ltd. with the FDA for Razor, Everest, U&c Liquid.
Device ID | K191902 |
510k Number | K191902 |
Device Name: | Razor, Everest, U&C Liquid |
Classification | Powder, Porcelain |
Applicant | U&C International Co., Ltd. RM 1F/2F, 13, Digital-ro 27-gil, Guro-gu Seoul, KR |
Contact | Jong-min Kim |
Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 1150 Roosevelt, STE 200 Irvine, CA 92620 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-07-16 |
Decision Date | 2019-10-11 |
Summary: | summary |