The following data is part of a premarket notification filed by Biotrack, Inc. with the FDA for Biotrack Immunochemistry Monitor.
Device ID | K900372 |
510k Number | K900372 |
Device Name: | BIOTRACK IMMUNOCHEMISTRY MONITOR |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | BIOTRACK, INC. 1058 HUFF AVE. Mountain View, CA 94043 |
Contact | Jill Findlay |
Correspondent | Jill Findlay BIOTRACK, INC. 1058 HUFF AVE. Mountain View, CA 94043 |
Product Code | JJQ |
CFR Regulation Number | 862.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-26 |
Decision Date | 1990-02-23 |