Pentax Medical of America, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pentax Medical of America, Inc. has 2 FDA 510(k) cleared medical devices. Based in Montvale, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pentax Medical of America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pentax Medical of America, Inc.
2 devices