Neoprobe Corp. - FDA 510(k) Cleared Devices
Recent clearances: NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES, NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Neoprobe Corp. Cardiovascular ✕
1 devices