FDA 510(k) Applications Submitted by NEOPROBE CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K050088 01/13/2005 QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER NEOPROBE CORP.
K962319 06/17/1996 NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES NEOPROBE CORP.
K971167 03/31/1997 NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES NEOPROBE CORP.


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