Bullfrog Micro-Infusion Device

FDA 510(k) K210339 · Mercator Medsystems, Inc.

Substantially Equivalent

510(k) numberK210339

Submission

Device name
Bullfrog Micro-Infusion Device
Applicant
Mercator Medsystems, Inc.
Emeryville, CA, US
Received
February 5, 2021
Decision date
August 2, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KRA – Catheter, Continuous Flush
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1210
Specialty
Cardiovascular

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More from Wallaby Medical

510(k)DeviceDecision
K161402Bullfrog Micro-Infusion DeviceKRA · Traditional 08/18/2016SE
K153501Bullfrog Micro-Infusion DeviceKRA · Traditional 04/15/2016SE
K131401Blowfish Transbronchial Micro-Infusion CatheterEOQ · Traditional 07/02/2013SE
K062752Mercator Microsyringe II Infusion CatheterKRA · Traditional 12/07/2006SE

Questions and answers

When was Bullfrog Micro-Infusion Device cleared by the FDA?

Bullfrog Micro-Infusion Device (K210339) received a 510(k) decision of Substantially Equivalent on August 2, 2021, 178 days after the submission was received.

What is the product code of K210339?

The FDA product code is KRA – Catheter, Continuous Flush, a Class II (moderate risk) device regulated under 21 CFR 870.1210.