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.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Hospitak, Inc. with 27 510(k) clearances. The most recent is a 510(k) clearance dated Feb 28, 1996: TRACH MASK MODEL (245, 246).
| Feb 28, 1996 | TRACH MASK MODEL (245, 246)K955483 · BYF | 510(k) clearances |
| Jan 31, 1996 | ILLUMINATORK954787 · CCW | 510(k) clearances |
| Aug 25, 1995 | WARM N WET HME W/LUER ADAPTERK953619 · BYD | 510(k) clearances |
| Aug 25, 1995 | WARM N WET HMEF W/LUER ADAPTERK953620 · BYD | 510(k) clearances |
| Nov 30, 1994 | DISPOSABLE BACTERIAL BREATHNG FILTERK915750 · CAH | 510(k) clearances |
| May 15, 1992 | AEROSOL DELIVERY SYSTEMSK920842 · LRD | 510(k) clearances |
| Feb 11, 1992 | DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNULK915228 · CCK | 510(k) clearances |
| Oct 26, 1987 | DISPOSABLE, MANUAL PULMONARY RESUSCITATORK873286 · BTM | 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
