Neoprobe Corp.
Neoprobe Corp. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2005.
Top product codes for Neoprobe Corp.
Recent clearances by Neoprobe Corp.
- K050088 — QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER
- K971167 — NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES
- K962319 — NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
- K942580 — NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES
- K915279 — NEOPROBE PORTABLE RADIOSCOPE DETECTOR
- K864263 — NEOPROBE PORTABLE RADIOISOTOPE DETECTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.