The following data is part of a premarket notification filed by Elan Diagnostics with the FDA for Atac Direct Ldl Reagent And Atac Direct Ldl Calibrator Kits.
Device ID | K020575 |
510k Number | K020575 |
Device Name: | ATAC DIRECT LDL REAGENT AND ATAC DIRECT LDL CALIBRATOR KITS |
Classification | System, Test, Low Density, Lipoprotein |
Applicant | ELAN DIAGNOSTICS 1075 W. LAMBERT RD., SUITE D Brea, CA 92821 |
Contact | Wynn Stocking |
Correspondent | Wynn Stocking ELAN DIAGNOSTICS 1075 W. LAMBERT RD., SUITE D Brea, CA 92821 |
Product Code | MRR |
CFR Regulation Number | 862.1475 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-02-21 |
Decision Date | 2002-04-12 |
Summary: | summary |