The following data is part of a premarket notification filed by Dentium Co., Ltd (ict Branch) with the FDA for Rainbow Mct.
Device ID | K200270 |
510k Number | K200270 |
Device Name: | Rainbow MCT |
Classification | X-ray, Tomography, Computed, Dental |
Applicant | Dentium Co., Ltd (ICT Branch) 76, Changnyong-daero 256beon-gil, Yeongtong-gu Suwon-si, KR 16229 |
Contact | Sangwoo Lee |
Correspondent | Dave Kim Mtech Group 7707 Fannin St. Ste 200, V111 Houston, TX 77054 |
Product Code | OAS |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-02-04 |
Decision Date | 2021-04-16 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08809460309836 | K200270 | 000 |