Parker notified of FDA 510(k) approval for nasotracheal intubation

In June, 2010, the U.S. FDA granted Parker Medical’s 510(k) application for clearance to sell Parker Flex-Tip tubes for nasal intubation in the U.S. This enabled us to close a large previous gap in our domestic endotracheal tube product line, and to better serve the needs of paramedics, emergency room physicians, dentist anesthesiologists, and oral surgeons who perform a substantial number of nasotracheal intubations.