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 The John Bunn Co. with 20 510(k) clearances. The most recent is a 510(k) clearance dated Apr 23, 1990: JOHN BUNN: MEDIX COMPACT TRAVELLER.
| Date | Record | Source |
|---|---|---|
| Apr 23, 1990 | JOHN BUNN: MEDIX COMPACT TRAVELLERK900854 · BTT | 510(k) clearances |
| Aug 18, 1988 | BUNN MODEL 50 OXYGEN FLOW CONTROLLERK883216 · NFB | 510(k) clearances |
| Sep 15, 1987 | BUNN CONCENTRATOR MODEL 2100 SERIESK873071 · CAW | 510(k) clearances |
| Mar 6, 1987 | BUNN MODEL 530 ASPIRATORK870094 · BTA | 510(k) clearances |
| Nov 7, 1986 | BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVEK861435 · CAW | 510(k) clearances |
| Aug 26, 1986 | BUNN MODEL 22 OXYGEN FLOW CONTROLLERK861199 · NFB | 510(k) clearances |
| Aug 7, 1986 | BUNN MODEL 510 MEDICATION COMPRESSORK862628 · BTI | 510(k) clearances |
| Feb 21, 1986 | BUNN LITE OXYGEN CONCENTRATORK855208 · CAW | 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
