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 14, 2026, FDA's public records list Transtracheal Systems with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 1999: TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000.
| Jul 12, 1999 | TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000K982943 · NFB | 510(k) clearances |
| Jul 23, 1998 | TRANSTRACHEAL AUGMENTED VENTILATION OXYGEN CONCENTRATOR MODEL NUMBER TTAV 1000K981078 · CAW | 510(k) clearances |
| Jun 17, 1998 | SCOOP 1K981080 · BTO | 510(k) clearances |
| Oct 23, 1996 | TRANSTRACHEAL DEMAND OXYGEN CONTROLLER (DOC-2000)K962944 · NFB | 510(k) clearances |
| Mar 1, 1991 | TRANSKINETICS RADO FREQ MULTI-LEAD TELE SYST 7200K904749 · DRQ | 510(k) clearances |
| Mar 1, 1991 | TRANSKINETICS INFRARED MULTI-LEAD TELE SYST 7100K904748 · DRG | 510(k) clearances |
| Aug 10, 1990 | MODIFIED SCOOP TRANSTRACHEAL CATHETERSK902281 · BTO | 510(k) clearances |
| Feb 3, 1986 | TRANSTRACHEAL SYSTEM-SCOOP-INSERTION TRAY-CATHETERK854252 · BTO | 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
