Mercator Medsystems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Mercator Medsystems, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Leandro, US.
Last cleared in 2021. Active since 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mercator Medsystems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mercator Medsystems, Inc.
5 devices
Cleared
Aug 02, 2021
Bullfrog Micro-Infusion Device
Cardiovascular
178d
Cleared
Aug 18, 2016
Bullfrog Micro-Infusion Device
Cardiovascular
90d
Cleared
Apr 15, 2016
Bullfrog Micro-Infusion Device
Cardiovascular
130d
Cleared
Jul 02, 2013
BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER
Ear, Nose, Throat
48d
Cleared
Dec 07, 2006
MERCATOR MICROSYRINGE II INFUSION CATHETER
Cardiovascular
84d