Last synced on 14 November 2025 at 11:06 pm

AcQGuide Flex with AcQCross QX, AcQGuide Mini with AcQCross QX

Page Type
Cleared 510(K)
510(k) Number
K193509
510(k) Type
Traditional
Applicant
Acutus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2020
Days to Decision
30 days
Submission Type
Summary

AcQGuide Flex with AcQCross QX, AcQGuide Mini with AcQCross QX

Page Type
Cleared 510(K)
510(k) Number
K193509
510(k) Type
Traditional
Applicant
Acutus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2020
Days to Decision
30 days
Submission Type
Summary