The following data is part of a premarket notification filed by Baxter Diagnostics, Inc. with the FDA for Stratus Folate Fluorometric Enzyme-linked Assay.
Device ID | K923286 |
510k Number | K923286 |
Device Name: | STRATUS FOLATE FLUOROMETRIC ENZYME-LINKED ASSAY |
Classification | Acid, Folic, Radioimmunoassay |
Applicant | BAXTER DIAGNOSTICS, INC. P.O. BOX 520672 Miami, FL 33152 |
Contact | Nancy A Hornbaker |
Correspondent | Nancy A Hornbaker BAXTER DIAGNOSTICS, INC. P.O. BOX 520672 Miami, FL 33152 |
Product Code | CGN |
CFR Regulation Number | 862.1295 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-06 |
Decision Date | 1992-09-17 |