Path Medical GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Path Medical GmbH - FDA 510(k) Cleared Devices
Recent clearances: QScreen, Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONE, ALGO 7i
6
Total
6
Cleared
0
Denied
Path Medical GmbH has 6 FDA 510(k) cleared medical devices. Based in Fort Collins, US.
Last cleared in 2022. Active since 2010. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Path Medical GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Path Medical GmbH
6 devices
Cleared
Aug 03, 2022
QScreen
Ear, Nose, Throat
197d
Cleared
Jun 22, 2022
Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced,...
Ear, Nose, Throat
257d
Cleared
Oct 14, 2021
ALGO 7i
Ear, Nose, Throat
178d
Cleared
Jun 09, 2014
SENTIERO
Ear, Nose, Throat
257d
Cleared
Jun 27, 2013
EARPROBE
Neurology
65d
Cleared
Jul 01, 2010
EARPROBE
Neurology
115d