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 J.S. Medical Associates with 18 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1993: VISI-SPOT.
| Nov 5, 1993 | VISI-SPOTK932752 · JTO | 510(k) clearances |
| Sep 8, 1993 | EYE SPOT IM TESTK932688 · KTN | 510(k) clearances |
| Aug 23, 1993 | EYE SPOT CRP TESTK932180 · DCN | 510(k) clearances |
| Aug 9, 1993 | ACCUTEX IM LATEX TESTK932551 · KTN | 510(k) clearances |
| Jul 28, 1993 | ACCUTEX BETA-HCG TESTK926112 · JHJ | 510(k) clearances |
| Dec 7, 1992 | ACCUTEX CRP LATEX TESTK924332 · DCK | 510(k) clearances |
| Dec 7, 1992 | ACCUTEX ASO LATEX TESTK924247 · GTQ | 510(k) clearances |
| Dec 1, 1992 | ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TESTK924036 · DHR | 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
