The following data is part of a premarket notification filed by Ok Biotech Co., Ltd. with the FDA for Ok Meter Blood Glucose Monitoring System.
Device ID | K063026 |
510k Number | K063026 |
Device Name: | OK METER BLOOD GLUCOSE MONITORING SYSTEM |
Classification | System, Test, Blood Glucose, Over The Counter |
Applicant | OK BIOTECH CO., LTD. NO. 58, FU-CHIUN ST. Hsin-chu City, TW 30067 |
Contact | Ke-min Jen |
Correspondent | Ke-min Jen OK BIOTECH CO., LTD. NO. 58, FU-CHIUN ST. Hsin-chu City, TW 30067 |
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 | 2006-10-02 |
Decision Date | 2007-02-09 |
Summary: | summary |