Announces Appointment of Michael Jesi
as Director, Quality & Regulatory Affairs
TEWKSBURY, MA, JANUARY 12, 2004 - Vasca, Inc.
, the developer, manufacturer and marketer of the LifeSite® Hemodialysis Access System, announced today the appointment of Michael Jesi
as Director of Quality & Regulatory Affairs for the Company. Mike joins Vasca with over 20 years of experience in the medical device market place having previously worked at Puritan-Bennett Corporation and Arrow International in several manufacturing, engineering, operations, R&D, quality and regulatory affairs roles/responsibilities.Most recently Mike was the Vice President of Product Development at endoVia Medical, Inc., a start-up medical device company developing minimally invasive surgical products and systems, where he led the product design, quality, regulatory and operations functions.
is a significant addition to the Vasca
..."Mike joins Vasca at an exciting time as we go to market in 2004 with a new indication for the use of the LifeSite System as a chronic (long term) hemodialysis access option."