AcQMap 3D Imaging and Mapping Catheter
K-Number: K170819 · 2017-10-16
Device Summary
Frequently Asked Questions
What is the AcQMap 3D Imaging and Mapping Catheter?
AcQMap 3D Imaging and Mapping Catheter is a medical device that received FDA 510(k) clearance on 2017-10-16. It is manufactured by Acutus Medical, Inc.. The 510(k) number is K170819.
When was AcQMap 3D Imaging and Mapping Catheter approved by the FDA?
AcQMap 3D Imaging and Mapping Catheter received FDA 510(k) clearance on 2017-10-16, under approval number K170819.
What company makes AcQMap 3D Imaging and Mapping Catheter?
AcQMap 3D Imaging and Mapping Catheter is manufactured by Acutus Medical, Inc..
What is the FDA product code for AcQMap 3D Imaging and Mapping Catheter?
The FDA product code for AcQMap 3D Imaging and Mapping Catheter is MTD.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.