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 Avatron, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 14, 1985: ANESTHESIA BREATHING CIRCUIT.
| Date | Record | Source |
|---|---|---|
| Jun 14, 1985 | ANESTHESIA BREATHING CIRCUITK851193 · CAI | 510(k) clearances |
| Feb 14, 1985 | AVA-MIST PORTABLE AIR COMPRESSORK844956 · BTI | 510(k) clearances |
| Aug 17, 1984 | AVA-NEB NEBULIZERK843102 · CCQ | 510(k) clearances |
| Jul 26, 1984 | AVATRON UNIVERSAL ADULT VOL. VENTILATORK842778 · BZO | 510(k) clearances |
| Jun 26, 1984 | AVATRON DISPOSABLE I.P.P.B. CIRUCITK842389 · BZO | 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
