The following data is part of a premarket notification filed by Ok Biotech Co., Ltd. with the FDA for Unistrip1 Generic Blood Glucose Test Strips.
Device ID | K162430 |
510k Number | K162430 |
Device Name: | UniStrip1 Generic Blood Glucose Test Strips |
Classification | System, Test, Blood Glucose, Over The Counter |
Applicant | OK BIOTECH CO., LTD. NO.91, SEC.2 GONGDAO 5TH ROAD Hsinchu City, TW 30070 |
Contact | Ke-min Jen |
Correspondent | Ke-min Jen OK BIOTECH CO., LTD. NO.91, SEC.2 GONGDAO 5TH ROAD Hsinchu City, TW 30070 |
Product Code | NBW |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-08-31 |
Decision Date | 2017-01-19 |
Summary: | summary |