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 Inhalation Plastics with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 13, 1995: SPIRO-FLEX.
| Jan 13, 1995 | SPIRO-FLEXK945565 · CAI | 510(k) clearances |
| Apr 15, 1992 | THERMO-FLOW SETK914686 · BTT | 510(k) clearances |
| Sep 10, 1990 | AEROMIST II NEBULIZERK901315 · CAF | 510(k) clearances |
| Apr 19, 1990 | FILT-R-ALL BACTERIAL/VIRAL FILTERK900990 · CAH | 510(k) clearances |
| Mar 15, 1990 | ANESTHESIA BREATHING CIRCUITK900594 · CAI | 510(k) clearances |
| Jan 22, 1990 | FILT-R-ALL BACTERIAL FILTERK896832 · CAH | 510(k) clearances |
| Feb 2, 1988 | STERILIZATION OF DEVICES BY RADIATIONK874659 · BTT | 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
