The following data is part of a premarket notification filed by Dfi Co., Ltd. with the FDA for Dus R-50s (urine Chemistry System).
Device ID | K171521 |
510k Number | K171521 |
Device Name: | DUS R-50S (Urine Chemistry System) |
Classification | Method, Enzymatic, Glucose (urinary, Non-quantitative) |
Applicant | DFI Co., Ltd. 388-25, Gomo-ro, Jillye-myeon, Gimhae-si Gyeongsangnam-do, KR 621-881 |
Contact | Bella Cho |
Correspondent | Ho Dong Yang Onbix Corporation #821 Samil Plaza, 14, Dogok-ro 1-gil, Gangnam-gu Seoul, KR 06523 |
Product Code | JIL |
Subsequent Product Code | CDM |
Subsequent Product Code | JFY |
Subsequent Product Code | JIN |
Subsequent Product Code | JIO |
Subsequent Product Code | JIR |
Subsequent Product Code | JJB |
Subsequent Product Code | JMT |
Subsequent Product Code | JRE |
Subsequent Product Code | KQO |
Subsequent Product Code | LJX |
CFR Regulation Number | 862.1340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-24 |
Decision Date | 2018-02-16 |
Summary: | summary |