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 14, 2026, FDA's public records list Amici, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 28, 2007: AEROSOL SYSTEM.
| Dec 28, 2007 | AEROSOL SYSTEMK063716 · CAF | 510(k) clearances |
| Mar 19, 1997 | THE SWIRLER NEBULIZERK952910 · CAF | 510(k) clearances |
| Nov 3, 1995 | THE SWIRLER AEROSOL SYSTEMK952893 · CAF | 510(k) clearances |
| Jan 14, 1991 | AMICI XENON ADMINISTRATION SETK903805 · IYT | 510(k) clearances |
| Jan 14, 1991 | AMICI KRYPTON ADMINISTRATION SYSTEM, MODIFICATIONK904684 · IYT | 510(k) clearances |
| Oct 3, 1990 | AMICI TRU-FIT SOFT PLASTIC MOUTHPIECEK903694 · IYT | 510(k) clearances |
| Feb 12, 1988 | AMICI KRYPTON ADMINISTRATION SYSTEM*K872920 · IYT | 510(k) clearances |
| Mar 3, 1987 | AMICI XENON REBREATHING SYSTEM*K865084 · IYT | 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
