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 15, 2026, FDA's public records list Inspiron with 20 510(k) clearances. The most recent is a 510(k) clearance dated Apr 9, 1986: INSPIRON DOUBLE SWIVEL TRACH ADAPTER.
| Apr 9, 1986 | INSPIRON DOUBLE SWIVEL TRACH ADAPTERK860838 · BZA | 510(k) clearances |
| Feb 4, 1985 | OXYGEN CONCENTRATORK850346 · CAW | 510(k) clearances |
| Oct 18, 1984 | VAPOR-PHASE HUMIDIFIER SYS-ADVANCEDK843932 · BTT | 510(k) clearances |
| Apr 5, 1984 | MANUAL RESUSCITATION SYSTEMK840935 · BTM | 510(k) clearances |
| Mar 30, 1984 | NEBULO 28 NEBULIZER KITK841158 · BTT | 510(k) clearances |
| Feb 17, 1984 | INSPIRATORY/EXPIRATORY MUSCLE EXERCISK840418 · BWF | 510(k) clearances |
| Feb 4, 1984 | INSPIRON LIQUID OXYGEN SYSTEMK834290 · BYJ | 510(k) clearances |
| Nov 15, 1977 | MANIFOLD & NEBULIZER, UNIVERSALK772068 · CAF | 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
