Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of TeleflexLabelled by claude-sonnet-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 Hudson Oxygen Therapy Sales Co. with 33 510(k) clearances. The most recent is a 510(k) clearance dated Sep 4, 1990: PEEP VALVE.
| Sep 4, 1990 | PEEP VALVEK902062 · BYE | 510(k) clearances |
| Jul 18, 1990 | MDI ADAPTORK900783 · CAF | 510(k) clearances |
| May 18, 1990 | IN-THE NEBULIZERK900470 · CAF | 510(k) clearances |
| Mar 30, 1990 | MANUAL RESUSCITATORK895589 · BTM | 510(k) clearances |
| Jan 9, 1990 | INFANT C.P.A.P. MONITORK896136 · CAP | 510(k) clearances |
| Oct 27, 1989 | VENTILARM II PORTABLE AIRWAY PRESSURE MONITORK895747 · CAP | 510(k) clearances |
| Oct 27, 1989 | CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZERK895231 · CAF | 510(k) clearances |
| May 5, 1989 | BACTERIA FILTERK890035 · CAH | 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
