The following data is part of a premarket notification filed by Gilford with the FDA for Advantage.
Device ID | K840120 |
510k Number | K840120 |
Device Name: | ADVANTAGE |
Classification | Analyzer, Chemistry (photometric, Discrete), For Clinical Use |
Applicant | GILFORD 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JJE |
CFR Regulation Number | 862.2160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-01-11 |
Decision Date | 1984-03-23 |