The following data is part of a premarket notification filed by Cliniqa Corporation with the FDA for Linical Immunology Calibration Verifiers Levels A-e For Beckman Coulter Synchron Cx Systems.
Device ID | K030074 |
510k Number | K030074 |
Device Name: | LINICAL IMMUNOLOGY CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER SYNCHRON CX SYSTEMS |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | CLINIQA CORPORATION 1432 SOUTH MISSION RD. Fallbrook, CA 92028 |
Contact | Carol Ruggiero |
Correspondent | Carol Ruggiero CLINIQA CORPORATION 1432 SOUTH MISSION RD. Fallbrook, CA 92028 |
Product Code | JIX |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-01-08 |
Decision Date | 2003-01-21 |