ProUroCare Medical Inc. announced the completion of a National Institute of Health and National Cancer Institute-supported clinical study. The study's purpose was to evaluate the ability of the company's ProUroScan imaging system to visualize and document abnormalities in the prostate detected or monitored by the digital rectal exam (DRE). The results of the clinical study will be submitted to the U.S. Food and Drug Administration (FDA) in support of a 510(k) application in the near future after third party validation of the data.

At the 2009 Annual Meeting of Shareholders of ProUroCare Medical Inc. held on August 11, 2009, the shareholders approved the adoption of the company's Amended Articles of Incorporation.

ProUroCare Medical Inc. announced that the second of the required three centers in its FDA clinical study of the ProUroScan Imaging System has completed its portion of the study. ProUroCare began the current study with the objective of enrolling at least 10 patients in three sites and having more than 40 patients enrolled overall. Since beginning, five clinical sites have been established, and as of last week, 44 patients have already been enrolled. The last of the three clinical studies to have 10 patients or more enrolled has only four patients remaining to meet their study objectives. ProUroCare expects to have 50 or more patients evaluated for their FDA submission, which is planned for fourth quarter 2009.