Automated Urinalysis System

FDA product code KQO · Class 1 · 11 devices · 51 reports · 8 devices named in recalls

• iQ200 Elite Plus (US) (2008 Version) (NA)

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  3 recalls2 reports
• iQ200 Sprint Pro (NA)/SPRINT w load/unload (NA)/SPRINT Pro w load/unload (NA)/Sprint P

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  3 recalls1 report
• iQ200 Select/Elite Pro (NA)

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  3 recalls0 reports
• iQ200 Select Plus Kit 2008 Analyzer (NA)/ Select Pro (NA)

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  2 recalls4 reports
• iChem Velocity Back-Integrated Velocity (NA)

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  1 recall15 reports
• Aution™ Hybrid AU-4050 Chemical Analyzer 14603

  Arkray USA, Inc. · Automated Urinalysis System
  1 recall4 reports
• iChem Velocity Elite/Stand-Alone Velocity (NA)

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  1 recall0 reports
• UA Win10 Kit C52900

  Beckman Coulter Ireland Inc. · Automated Urinalysis System
  1 recall0 reports
• cobas u 411 Urine Analyzer 4906969001

  Roche Diagnostics GmbH · AUTOMATED URINALYSIS SYSTEM
  16 reports
• cobas u 601 urine analyzer 06390498001

  Roche Diagnostics GmbH · AUTOMATED URINALYSIS SYSTEM
  8 reports
• Clinitek Atlas® 10 Reagent PAK for Urine Chemistry 10311120

  Siemens Healthcare Diagnostics Inc. · AUTOMATED URINALYSIS SYSTEM
  1 report