The following data is part of a premarket notification filed by American Dade with the FDA for Paramax Bilirubin Calibrators.
Device ID | K833005 |
510k Number | K833005 |
Device Name: | PARAMAX BILIRUBIN CALIBRATORS |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | AMERICAN DADE 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JIX |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-08-12 |
Decision Date | 1983-11-14 |