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FDA 510(k)

AcQMap 3D Imaging and Mapping Catheter

K-Number: K170819 · 2017-10-16

Decision Date2017-10-16
Product CodeMTD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AcQMap 3D Imaging and Mapping Catheter is a medical device manufactured by Acutus Medical, Inc.. It received FDA 510(k) clearance on 2017-10-16 under approval number K170819. The device is classified under product code MTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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