The following data is part of a premarket notification filed by I-sens, Inc. with the FDA for Caresens N Feliz Blood Glucose Monitoring System, Caresens N Feliz Bt Blood Glucose Monitoring System.
Device ID | K201394 |
510k Number | K201394 |
Device Name: | CareSens N Feliz Blood Glucose Monitoring System, CareSens N Feliz BT Blood Glucose Monitoring System |
Classification | System, Test, Blood Glucose, Over The Counter |
Applicant | i-SENS, Inc. 43, Banpo-daero 28-gil, Seocho-gu Seoul, KR 06646 |
Contact | Joon Ho Jung |
Correspondent | Joon Ho Jung i-SENS, Inc. 43, Banpo-daero 28-gil, Seocho-gu Seoul, KR 06646 |
Product Code | NBW |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-05-27 |
Decision Date | 2021-10-05 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10885325001690 | K201394 | 000 |
10885325001683 | K201394 | 000 |