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 Applied Polytechnology, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 4, 1986: FILTRA-CHECK-UTI.
| Apr 4, 1986 | FILTRA-CHECK-UTIK860483 · JXA | 510(k) clearances |
| Nov 29, 1984 | BACTERIURIA DETECT. DEVICE APTEK IIK843834 · JXA | 510(k) clearances |
| Nov 29, 1984 | BACTERIURIA DETECT DEVICE, MULTI SAMPLERK843833 · JXA | 510(k) clearances |
| Sep 27, 1984 | URINE TRANSPORT KITK843359 · JTW | 510(k) clearances |
| Sep 11, 1984 | INDOLE SPOT TEST KIT 270-25K843316 · JTO | 510(k) clearances |
| Apr 19, 1984 | RAPID IMMUNO-ASSAY SYSK840257 · LLG | 510(k) clearances |
| Jan 13, 1984 | REVERSE-FLOW SYSTEMK834264 · JTA | 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
