Pentax Medical - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Pentax Medical has 6 FDA 510(k) cleared medical devices. Based in Montvale, US.
Historical record: 6 cleared submissions from 2013 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pentax Medical Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pentax Medical
6 devices
Cleared
Oct 21, 2019
PENTAX Medical ED-3490TK Video Duodenoscope
Gastroenterology & Urology
60d
Cleared
Jul 18, 2018
PENTAX Medical VIVIDEO ENT Videoscope Solution
Ear, Nose, Throat
470d
Cleared
Apr 05, 2018
PENTAX Medical EPK-3000 Video Imaging System
Ear, Nose, Throat
261d
Cleared
Feb 07, 2018
PENTAX MEDICAL ED-3490TK, Video Duodenoscope
Gastroenterology & Urology
649d
Cleared
Sep 20, 2017
PENTAX Medical ED34-i10T, Video Duodenoscope
Gastroenterology & Urology
272d
Cleared
Apr 10, 2013
PENTAX EPK-I5010 VIDEO PROCESSOR
Gastroenterology & Urology
240d