The following data is part of a premarket notification filed by Coulter Corp. with the FDA for Coulter Albumin Reagent.
Device ID | K901268 |
510k Number | K901268 |
Device Name: | COULTER ALBUMIN REAGENT |
Classification | Bromcresol Green Dye-binding, Albumin |
Applicant | COULTER CORP. 745 WEST 83RD ST. Hialeah, FL 33014 |
Contact | A Richardson-jones |
Correspondent | A Richardson-jones COULTER CORP. 745 WEST 83RD ST. Hialeah, FL 33014 |
Product Code | CIX |
CFR Regulation Number | 862.1035 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-16 |
Decision Date | 1990-05-30 |