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 Amcor and its 2 subsidiaries with 14 510(k) clearances. The most recent is a 510(k) clearance dated Oct 30, 1995: SLANT/FIN HEPA CLEAR.
| Date | Record | Source |
|---|---|---|
| Oct 30, 1995 | SLANT/FIN HEPA CLEARK953536 · FRF | 510(k) clearances |
| Oct 19, 1995 | MEDI-OXIDE STERILZATION POUCH FROM MEDI-PLUSK953749 · KCT | 510(k) clearances |
| Jan 25, 1989 | BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.K885019 · FRG | 510(k) clearances |
| Oct 18, 1982 | SPECIMEN ADAPTORK822557 · BYZ | 510(k) clearances |
| Oct 18, 1982 | CRITICAL MEASUREMENT UNITK822556 · BYZ | 510(k) clearances |
| Jan 21, 1981 | SUCTION PROBEK803206 · JOL | 510(k) clearances |
| Dec 20, 1977 | SUCTION CANISTERK771737 · GCX | 510(k) clearances |
| Sep 28, 1977 | MALE URINALK771738 · FNP | 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
