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 13, 2026, FDA's public records list Barosense with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 10, 2012: BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE.
| Date | Record | Source |
|---|---|---|
| Sep 10, 2012 | BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIEK120126 · FED | 510(k) clearances |
| Feb 17, 2012 | ACE STAPLER AND CARTRIDGEK120147 · OCW | 510(k) clearances |
| Jun 3, 2011 | ACE STAPLER AND CARTRIDGEK110829 · OCW | 510(k) clearances |
| May 11, 2010 | ACE STAPLER, MODEL F0031K082044 · OCW | 510(k) clearances |
| May 22, 2009 | BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034K082589 · FED | 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
