The following data is part of a premarket notification filed by I-sens, Inc. with the FDA for Nocoding1 Plus Blood Glucose Monitoring System.
Device ID | K160742 |
510k Number | K160742 |
Device Name: | NoCoding1 Plus Blood Glucose Monitoring System |
Classification | System, Test, Blood Glucose, Over The Counter |
Applicant | i-SENS, INC. 43, BANPO-DAER0 28-GIL, SEOCHO-GU Seoul, KR 06646 |
Contact | Joon Ho Jung |
Correspondent | Joon Ho Jung i-SENS, INC. 43, BANPO-DAER0 28-GIL, SEOCHO-GU Seoul, KR 06646 |
Product Code | NBW |
Subsequent Product Code | CGA |
Subsequent Product Code | JJX |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-17 |
Decision Date | 2016-12-16 |
Summary: | summary |