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 Thompson Respiration Products, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 26, 1982: MODEL M3000XA VENTILATOR SPECIFICA.
| Jul 26, 1982 | MODEL M3000XA VENTILATOR SPECIFICAK822103 · CBK | 510(k) clearances |
| Jan 22, 1979 | PRESSURE ALARMK782174 · CAP | 510(k) clearances |
| Dec 18, 1978 | ALARM UNIT, BATTERY OPERATEDK781158 · BZQ | 510(k) clearances |
| Dec 13, 1978 | VENTILATOR, MINILUNGK781160 · CBK | 510(k) clearances |
| Dec 12, 1978 | VENTILATOR, PRESSUREK781159 · CBK | 510(k) clearances |
| Dec 11, 1978 | RESPIRATOR, BANTAM MODELK781161 · CBK | 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
