Medical device 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 Neoprobe Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 8, 2005: QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER.
| Date | Record | Source |
|---|---|---|
| Feb 8, 2005 | QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZERK050088 · DPW | 510(k) clearances |
| Jun 26, 1997 | NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIESK971167 · IZD | 510(k) clearances |
| Sep 13, 1996 | NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIESK962319 · IZD | 510(k) clearances |
| Feb 9, 1995 | NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIESK942580 · IZD | 510(k) clearances |
| Jun 10, 1992 | NEOPROBE PORTABLE RADIOSCOPE DETECTORK915279 · IZD | 510(k) clearances |
| Dec 29, 1986 | NEOPROBE PORTABLE RADIOISOTOPE DETECTORK864263 · IZD | 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
