The following data is part of a premarket notification filed by Bio-rad with the FDA for Coda Automated Eia Analyzer.
Device ID | K972024 |
510k Number | K972024 |
Device Name: | CODA AUTOMATED EIA ANALYZER |
Classification | Analyzer, Enzyme, For Clinical Use |
Applicant | BIO-RAD 4000 ALFRED NOBEL DR. Hercules, CA 94547 -1803 |
Contact | John W Nelson |
Correspondent | John W Nelson BIO-RAD 4000 ALFRED NOBEL DR. Hercules, CA 94547 -1803 |
Product Code | JJI |
CFR Regulation Number | 862.2500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-02 |
Decision Date | 1997-07-30 |
Summary: | summary |