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

AcQCross Qx Integrated Transseptal Dilator/Needle

K Number: K220047 · Decision Feb 8, 2022
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
24
Review Days
34

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Basic Information

Device Name
AcQCross Qx Integrated Transseptal Dilator/Needle
K Number
K220047
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acutus Medical, Inc.
Date Received
January 5, 2022
Decision Date
February 8, 2022
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
DYB Introducer, Catheter

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Other Clearances by Acutus Medical, Inc.

K Number Device Name
K233691 FlexCath Cross Transseptal Solution
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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
K212345 AcQMap High Resolution Imaging and Mapping System
K210680 AcQMap High Resolution Imaging and Mapping System
K211100 AcQGuide MAX Steerable Sheath
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