The following data is part of a premarket notification filed by Fujirebio Diagnostics, Inc with the FDA for Fdi Glucose Control Solutions.
Device ID | K102260 |
510k Number | K102260 |
Device Name: | FDI GLUCOSE CONTROL SOLUTIONS |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | FUJIREBIO DIAGNOSTICS, INC 940 CROSSROADS BLVD. Seguin, TX 78155 |
Contact | Kent Pruett |
Correspondent | Kent Pruett FUJIREBIO DIAGNOSTICS, INC 940 CROSSROADS BLVD. Seguin, TX 78155 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-10 |
Decision Date | 2010-09-24 |
Summary: | summary |