Phoenix Diagnostics, Inc.
Phoenix Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2002.
Top product codes for Phoenix Diagnostics, Inc.
Recent clearances by Phoenix Diagnostics, Inc.
- K023268 — PHOENIX ISE STANDARD A,B AND C FOR ROCHE/AVL SYSTEMS
- K020364 — PHOENIX ISE REAGENTS FOR BECKMAN CX SYSTEMS
- K020148 — pHoenix ISE Reagents FOR Olympus AU Chemistry Systems
- K020129 — PHOENIX ELETROLYTE CALIBRATION SET FOR THE ROCHE COBAS ISE MODULE
- K013451 — PHOENOIX ISE REAGENTS FOR ROCHE HITACHI, MODELS 700/900 SERIES
- K012987 — PHOENIX ELECTROLYTE CALIBRATION SET FOR THE MEDICAL EASYLYTE CALCIUM ANALYZER
- K012509 — PHOENIX ELECTROLYTE CALIBRATION SET FOR THE DADE/BEHRING/BEHRING DIMENSION CHEMISTRY SYSTEM
- K960592 — ELECTROLYTE STANDARDS
- K945860 — SPECTRUM CO-OXIMETER LINEARITY CONTROL
- K920285 — BLOOD GAS/ISE LINEARITY CONTROL
- K912718 — ENZYME LINEARITY CONTROL
- K904075 — CLINICAL CHEMISTRY CONTROL
- K902675 — MULTI ANALYTE MIXTURE, CALIBRATORS
- K902094 — BLOOD GAS/ISE CONTROLS
- K902616 — BILIRUBIN CONTROL
- K902095 — BLOOD GAS/ELECTROLYTE/CO-OXIMETER CONTROLS
- K902267 — BLOOD GASES/PC02, PO2 ANALYSIS PRODUCTS
- K901985 — BLOOD GAS CONTROLS
- K902266 — ELECTROLYTE CONTROLS (ASSAYED AND UNASSAYED)
- K901976 — BLOOD GAS/CO-OXIMETRY CONTROL
- K901986 — CO-OXIMETER CONTROLS
Data sourced from openFDA. This site is unofficial and independent of the FDA.