Good morning, and thank you for joining us on today's call. We certainly have more good news as can be seen by the announcement this morning. Last quarter, I reported was our top revenue quarter. But today, I once again point out that this Q2 2023 is now our top ever revenue quarter. Q2 also marks our 8th consecutive record revenue quarter. As this morning's press release announced, second quarter 2023 revenue came in at $16.1 million, representing a 27% increase over second quarter 2022. GAAP diluted earnings per share for the second quarter were $0.33. Non-GAAP diluted earnings per share for the second quarter of 2023 were $0.36 per share, a 38% increase over Q2 2022. Once again, I'm very proud of the fantastic efforts of the entire team. Revenue and order growth has been strong for all product lines. The MRI patient vital signs monitor continued to make deep inroads into the competitive base with the growth of pump orders also very inspiring further confidence in our ability to execute. As with last quarter, we again feel comfortable in raising our guidance for the year, which you will learn of in a moment. Our sales team has maintained a high level of performance as evidenced by strong customer demand for our products. Our total backlog built through Q2 continues to be at a robust level. Strong backlog provides excellent visibility and allows us to maneuver and reallocate resources as supply issues may arise. Those supply chain issues continue to become less and less of a concern. We still must be cautious. One trade of our caution can be seen in our inventory buildup. Once again, I'd like to provide progress toward our FDA efforts surrounding the new 3870 MRIV pump. As reported last quarter, we have since then had a continuing dialogue with the FDA. One such interaction was a face-to-face meeting at FDA in the D.C. area, which was, we understand, may have been the first device company face-to-face since COVID. FDA personnel continue to work remotely, which we could plainly see by the very few people in that facility during our visit. But there now have been some positions filled. That of the lead reviewer and the director -- or assistant director, I should say, of the infusion devices, whom we met. And we're hopeful that these new people will come up to speed regarding IV pumps, and that as we refile, they will have the ability to address our 510(k) expeditiously. Massive often repeat testing is underway for us, and we expect to finalize and submit this repeated 510(k) in Q1 of next year. As background, FDA has been working and clearing mostly repeat 510(k)s from other hospital IV pump suppliers, with recently Fresenius and Baxter just having been cleared. And although we see a new recall happening earlier this week for yet another IV pump player, which may likely require a repeat 510(k) for them as well, so this adds to the staffing loads upon the FDA people. So we must take a conservative view that the current MRIV pump will remain strong in sales for our revenue stream into 2025. Now I'd like to recap our recent Q2 performance and indicate our confidence that this upward trajectory will continue. Therefore, we now announce an increase in our guidance with the expectation of revenue for the year at $64.5 million to $65.5 million. We also raised the forecasted annual GAAP diluted earnings per share to $1.25 to $1.28, and non-GAAP diluted earnings is a raise to $1.37 to $1.40. For the third quarter 2023, third quarter typically being our weakest, we expect to report revenue of $16.1 million to $16.3 million, GAAP diluted earnings per share of $0.33 to $0.35 and non-GAAP diluted earnings per share of $0.36 to $0.38. Now I'd like to turn the call over to Jack Glenn, our CFO, to review the fiscal results of the quarter. Thanks, Jack.