The following data is part of a premarket notification filed by Baxter Diagnostics, Inc. with the FDA for Stratus Estradiol Fluorometric Enzyme Immunoassay.
Device ID | K933464 |
510k Number | K933464 |
Device Name: | STRATUS ESTRADIOL FLUOROMETRIC ENZYME IMMUNOASSAY |
Classification | Radioimmunoassay, Estradiol |
Applicant | BAXTER DIAGNOSTICS, INC. SCIENTIFIC PRODUCTS DIV. 1430 WAUKEGAN RD. Mcgaw Park, IL 60085 |
Contact | Betty Hernandez-labadie |
Correspondent | Betty Hernandez-labadie BAXTER DIAGNOSTICS, INC. SCIENTIFIC PRODUCTS DIV. 1430 WAUKEGAN RD. Mcgaw Park, IL 60085 |
Product Code | CHP |
CFR Regulation Number | 862.1260 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-07-16 |
Decision Date | 1993-10-22 |