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Path Medical GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220139QScreenAugust 3, 2022
K213345Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONEJune 22, 2022
K211147ALGO 7iOctober 14, 2021
K133012SENTIEROJune 9, 2014
K131141EARPROBEJune 27, 2013
K100661EARPROBEJuly 1, 2010