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 Gastrotech, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 3, 1989: SYRINGE INJECTION GUN DELIVERY KITS.
| Oct 3, 1989 | SYRINGE INJECTION GUN DELIVERY KITSK890658 · LRO | 510(k) clearances |
| May 31, 1989 | ESOPHAGEAL OVERTUBEK890629 · FED | 510(k) clearances |
| Aug 23, 1988 | GASTROSTOMY FEEDING TUBEK883336 · KNT | 510(k) clearances |
| Aug 23, 1988 | PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING TUBEK883351 · KNT | 510(k) clearances |
| Aug 6, 1986 | SYRINGE INJECTION GUNK862853 · | 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
