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 Alltek with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 5, 1985: I.V. WATCH.
| Date | Record | Source |
|---|---|---|
| Dec 5, 1985 | I.V. WATCHK854172 · FPB | 510(k) clearances |
| May 30, 1985 | PEDIATRIC IV WATCHK852030 · FPB | 510(k) clearances |
| May 30, 1985 | I.V. WATCHK852029 · FPB | 510(k) clearances |
| Jun 19, 1984 | MANUAL IRRIGATING/ASPIRATING UNITK840495 · HQC | 510(k) clearances |
| May 11, 1984 | FILTRARE TM ALLVENT TMK834376 · FPB | 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
