The following data is part of a premarket notification filed by Mallinckrodt Critical Care with the FDA for Combined Glucose And Bun Standards.
Device ID | K802825 |
510k Number | K802825 |
Device Name: | COMBINED GLUCOSE AND BUN STANDARDS |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | MALLINCKRODT CRITICAL CARE 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 | 1980-11-10 |
Decision Date | 1980-12-11 |