Medical device makerLabelled 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 Pacific Device, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1997: VITALMIX PLUS EMPTY I.V. CONTAINER.
| Date | Record | Source |
|---|---|---|
| Nov 5, 1997 | VITALMIX PLUS EMPTY I.V. CONTAINERK972464 · KPE | 510(k) clearances |
| Jul 2, 1993 | TRANSFER SETK923782 · LHI | 510(k) clearances |
| Aug 28, 1991 | INTRAVASCULAR ADMINISTRATION SETSK912860 · FPA | 510(k) clearances |
| Jul 30, 1991 | MECONIUM ASPIRATIONK912596 · BSY | 510(k) clearances |
| Jul 2, 1990 | VITALMIX (SET & BAG)K902482 · LHI | 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
