3M Avi, Inc.
3M Avi, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1993.
Top product codes for 3M Avi, Inc.
Recent clearances by 3M Avi, Inc.
- K912069 — AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET
- K912589 — AVI MODEL 840D DUAL CHANNEL INFUSION PUMP
- K912590 — AVI MODEL 400D INFUSION PUMP
- K912591 — AVI MICRO 210D INFUSION PUMP
- K912875 — AVI MODEL 270CI INFUSION PUMP
- K912738 — AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELS
- K912031 — AVI MODEL 870 DUAL CHANNEL INFUSION PUMP
- K904979 — AVI MODEL 600 SYRINGE PUMP, MODIFICATION
- K902858 — AVI MODEL 4206 MANIFOLD CHECKVALVE IV ADMIN. SET
- K903782 — AVI MODEL 270CM INFUSION PUMP
- K903783 — AVI MICRO 275CM INFUSION PUMP
- K903785 — AVI MODEL 400CM INFUSION PUMP
- K903786 — AVI MICRO 845 DUAL CHANNEL INFUSION PUMP
- K903787 — AVI MODEL 470CM INFUSION PUMP
- K903788 — AVI MICRO 285CM INFUSION PUMP
- K903781 — AVI MODEL 880 DUAL CHANNEL INFUSION PUMP
- K903784 — AVI MODEL 480CM INFUSION PUMP
- K903789 — AVI MICRO 885 DUAL CHANNEL INFUSION PUMP
Data sourced from openFDA. This site is unofficial and independent of the FDA.