The following data is part of a premarket notification filed by Cliniqa Corporation with the FDA for Linical Esoterics Calibration Verifiers Levels A-e For Beckman Coulter Synchron Analyzers.
Device ID | K032074 |
510k Number | K032074 |
Device Name: | LINICAL ESOTERICS CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER SYNCHRON ANALYZERS |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | CLINIQA CORPORATION 1432-B SOUTH MISSION RD. Fallbrook, CA 92028 |
Contact | Carol Ruggiero |
Correspondent | Carol Ruggiero CLINIQA CORPORATION 1432-B SOUTH MISSION RD. Fallbrook, CA 92028 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-07-07 |
Decision Date | 2003-10-21 |