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

AcQMap High Resolution Imaging and Mapping System

K Number: K181577 · Decision Feb 7, 2019
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
403
Applicant Total
20
Review Days
237

Basic Information

Device Name
AcQMap High Resolution Imaging and Mapping System
K Number
K181577
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acutus Medical, Inc.
Date Received
June 15, 2018
Decision Date
February 7, 2019
Product Code
DQK
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
DQK Computer, Diagnostic, Programmable

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