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AcQGuide Flex with AcQCross QX, AcQGuide Mini with AcQCross QX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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