FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AcQMap 3D Imaging and Mapping Catheter

K Number: K170819 · Decision Oct 16, 2017
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
33
Applicant Total
24
Review Days
210

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Basic Information

Device Name
AcQMap 3D Imaging and Mapping Catheter
K Number
K170819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acutus Medical, Inc.
Date Received
March 20, 2017
Decision Date
October 16, 2017
Product Code
MTD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MTD Catheter, Intracardiac Mapping, High-Density Array

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Other Clearances by Acutus Medical, Inc.

K Number Device Name
K233691 FlexCath Cross Transseptal Solution
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K230606 AcQMap® High Resolution Imaging and Mapping System
K222209 AcQMap High Resolution Imaging and Mapping System
K220784 AcQMap High Resolution Imaging and Mapping System
K210766 AcQMap 3D Imaging and Mapping Catheter, Model 900009
K221044 AcQGuide® VUE Steerable Sheath
K220047 AcQCross Qx Integrated Transseptal Dilator/Needle
K212345 AcQMap High Resolution Imaging and Mapping System
K210680 AcQMap High Resolution Imaging and Mapping System
Search all 24 clearances from Acutus Medical, Inc. →