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 |