The following data is part of a premarket notification filed by Abbott Laboratories with the FDA for Architect Total Bilirubin.
Device ID | K121985 |
510k Number | K121985 |
Device Name: | ARCHITECT TOTAL BILIRUBIN |
Classification | Diazo Colorimetry, Bilirubin |
Applicant | ABBOTT LABORATORIES 1921 HURD DRIVE Irving, TX 75038 |
Contact | Linda Morris |
Correspondent | Linda Morris ABBOTT LABORATORIES 1921 HURD DRIVE 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 | 2012-07-06 |
Decision Date | 2013-02-01 |
Summary: | summary |