Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Applied Medical Technologies with 24 510(k) clearances. The most recent is a 510(k) clearance dated Aug 17, 1998: A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICE.
| Aug 17, 1998 | A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICEK971434 · KNT | 510(k) clearances |
| Feb 9, 1998 | PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIESK972478 · KNT | 510(k) clearances |
| Dec 19, 1997 | AMT BALLOON STOMA MEASURING DEVICES, AMT BALLOON MEASURING DEVICE, AMT BALLOON MEASURING DEVICE WITH STOP VALVE, AMY BAEK973893 · KNT | 510(k) clearances |
| Nov 7, 1997 | LOW PROFILE FEEDING SET ACCESSORYK971757 · KNT | 510(k) clearances |
| Jul 21, 1997 | CAUTERIZATION SMOKE EVACUATORK971758 · GEI | 510(k) clearances |
| Sep 17, 1996 | DOMED PERCUTANEOUS ENDOSCOPIC GASTROSTOMY(P.E.G.) FEEDING TUBEK961345 · KNT | 510(k) clearances |
| Mar 21, 1996 | ENDOSCOPIC ACCESS DEVICEK960232 · GCJ | 510(k) clearances |
| Oct 12, 1995 | GASTROINTESTINAL TUBES & ACCESSORIESK945618 · KNT | 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
