The following data is part of a premarket notification filed by Hass Corp. with the FDA for Amber Mill Q Series & Amber Mill Direct Series.
Device ID | K202952 |
510k Number | K202952 |
Device Name: | Amber Mill Q Series & Amber Mill Direct Series |
Classification | Powder, Porcelain |
Applicant | HASS Corp. 77-14, Gwahakdanji-ro Gangneung-si, KR 25452 |
Contact | Yongsu 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 | 2020-09-30 |
Decision Date | 2021-08-26 |