Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of 3MLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list 3M Avi with 18 510(k) clearances. The most recent is a 510(k) clearance dated Oct 14, 1993: AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET.
| Date | Record | Source |
|---|---|---|
| Oct 14, 1993 | AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SETK912069 · FPA | 510(k) clearances |
| Oct 17, 1991 | AVI MODEL 840D DUAL CHANNEL INFUSION PUMPK912589 · FRN | 510(k) clearances |
| Oct 17, 1991 | AVI MODEL 400D INFUSION PUMPK912590 · FRN | 510(k) clearances |
| Sep 6, 1991 | AVI MICRO 210D INFUSION PUMPK912591 · FRN | 510(k) clearances |
| Aug 20, 1991 | AVI MODEL 270CI INFUSION PUMPK912875 · FRN | 510(k) clearances |
| Aug 12, 1991 | AVI VOLUMETRIC INFUSION PUMPS-VARIOUS MODELSK912738 · FRN | 510(k) clearances |
| Jun 18, 1991 | AVI MODEL 870 DUAL CHANNEL INFUSION PUMPK912031 · FRN | 510(k) clearances |
| Jan 15, 1991 | AVI MODEL 600 SYRINGE PUMP, MODIFICATIONK904979 · FRN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
