The following data is part of a premarket notification filed by Abbott Laboratories with the FDA for Total Bilirubin.
Device ID | K022339 |
510k Number | K022339 |
Device Name: | TOTAL BILIRUBIN |
Classification | Diazo Colorimetry, Bilirubin |
Applicant | ABBOTT LABORATORIES 1920 HURD DR. Irving, TX 75038 |
Contact | Michele Smith-waheed |
Correspondent | Michele Smith-waheed ABBOTT LABORATORIES 1920 HURD DR. Irving, TX 75038 |
Product Code | CIG |
CFR Regulation Number | 862.1110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-07-18 |
Decision Date | 2002-09-13 |
Summary: | summary |