The following data is part of a premarket notification filed by Infopia Co., Ltd with the FDA for Gluneo Blood Glucose Monitoring System, And Professional Blood Glucose Monitoring System.
Device ID | K130181 |
510k Number | K130181 |
Device Name: | GLUNEO BLOOD GLUCOSE MONITORING SYSTEM, AND PROFESSIONAL BLOOD GLUCOSE MONITORING SYSTEM |
Classification | System, Test, Blood Glucose, Over The Counter |
Applicant | INFOPIA CO., LTD 1515 E KATELLA AVE UNIT 2115 Anaheim, CA 92805 |
Contact | Priscilla Chung |
Correspondent | Priscilla Chung INFOPIA CO., LTD 1515 E KATELLA AVE UNIT 2115 Anaheim, CA 92805 |
Product Code | NBW |
Subsequent Product Code | JJX |
Subsequent Product Code | JQP |
Subsequent Product Code | LFR |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-01-25 |
Decision Date | 2013-07-31 |
Summary: | summary |