CANNULA, SINUS

FDA product code KAM · Class 1 · 3 devices · 4 reports · 0 devices named in recalls

• RELIEVA FLEX GC090RF

  Acclarent, Inc. · CANNULA, SINUS
  2 reports
• RELIEVA FLEX GC070CRF

  Acclarent, Inc. · CANNULA, SINUS
  1 report
• RELIEVA FLEX GC110RF

  Acclarent, Inc. · CANNULA, SINUS
  1 report