The following data is part of a premarket notification filed by Bionostics, Inc. with the FDA for Glucose Meter-check Solution For Infopia.
Device ID | K113764 |
510k Number | K113764 |
Device Name: | GLUCOSE METER-CHECK SOLUTION FOR INFOPIA |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | BIONOSTICS, INC. 7 JACKSON RD. Devens, MA 01434 |
Contact | Randy Byrd |
Correspondent | Randy Byrd BIONOSTICS, INC. 7 JACKSON RD. Devens, MA 01434 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-12-21 |
Decision Date | 2012-01-30 |
Summary: | summary |