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 15, 2026, FDA's public records list Applied Medical Devices with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 19, 1984: PERCUTANEOUS ASPIRATION BIOPSY TRAY.
| Dec 19, 1984 | PERCUTANEOUS ASPIRATION BIOPSY TRAYK843885 · | 510(k) clearances |
| Dec 13, 1984 | STERILE PERCUTANEOUS TRANSHEPATIC CHOLANK843883 · | 510(k) clearances |
| Dec 13, 1984 | GENERAL UTILITY TRAY SYSTEMK843884 · | 510(k) clearances |
| Aug 16, 1984 | ACCU-CULT FECAL OCCULT BLOOD TESTK840904 · KHE | 510(k) clearances |
| Jul 23, 1984 | ULTRASOUND PROBE COVERS-STERILEK842591 · IYO | 510(k) clearances |
| May 30, 1984 | TRANSTHORACIC/TRANSABDOMINAL-TRAYK833720 · GDM | 510(k) clearances |
| Apr 13, 1984 | CHEMONUCLEOLYSIS/DISCOGRAPHY TRAYK840334 · FMI | 510(k) clearances |
| Feb 9, 1984 | PREPACELL-STERILE-BONE MARROW ASPIRK833438 · KDD | 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
