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Mercator Medsystems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210339Bullfrog Micro-Infusion DeviceAugust 2, 2021
K161402Bullfrog Micro-Infusion DeviceAugust 18, 2016
K153501Bullfrog Micro-Infusion DeviceApril 15, 2016
K131401BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETERJuly 2, 2013
K062752MERCATOR MICROSYRINGE II INFUSION CATHETERDecember 7, 2006