The following data is part of a premarket notification filed by Baxter Diagnostics, Inc. with the FDA for Dade(r) Tumor Marker Control.
Device ID | K924919 |
510k Number | K924919 |
Device Name: | DADE(R) TUMOR MARKER CONTROL |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | BAXTER DIAGNOSTICS, INC. P.O. BOX 520672 Miami, FL 33152 |
Contact | Charla Issitt |
Correspondent | Charla Issitt BAXTER DIAGNOSTICS, INC. P.O. BOX 520672 Miami, FL 33152 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-29 |
Decision Date | 1993-08-05 |