The following data is part of a premarket notification filed by Stanbio Laboratory with the FDA for Stanbio Bilirubin Test Set.
Device ID | K810055 |
510k Number | K810055 |
Device Name: | STANBIO BILIRUBIN TEST SET |
Classification | Diazo Colorimetry, Bilirubin |
Applicant | STANBIO LABORATORY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CIG |
CFR Regulation Number | 862.1110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-01-13 |
Decision Date | 1981-02-02 |