Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 13, 2026, FDA's public records list Immunoprobe with 14 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 1997: ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM.
| Date | Record | Source |
|---|---|---|
| Dec 22, 1997 | ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEMK972406 · GOD | 510(k) clearances |
| Jul 14, 1997 | MYCOPLASMA IGG ELISA TEST SYSTEMK971393 · LJZ | 510(k) clearances |
| Aug 19, 1996 | MPO ELISA TEST SYSTEMK961765 · MOB | 510(k) clearances |
| Aug 19, 1996 | PR-3 ELISA TEST SYSTEMK961764 · MOB | 510(k) clearances |
| Apr 29, 1996 | EBNA IGG EIA TEST SYSTEMK951549 · LLM | 510(k) clearances |
| Feb 9, 1996 | CARDIOLIPIN IGG EIA TEST KITK952523 · MID | 510(k) clearances |
| Feb 9, 1996 | CARDIOLIPIN IGA EIA TEST SYSTEMK952522 · MID | 510(k) clearances |
| Feb 9, 1996 | CARDIOLIPIN IGM EIA TEST SYSTEMK952521 · MID | 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
