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ABMD Software

Page Type
Cleared 510(K)
510(k) Number
K213760
510(k) Type
Traditional
Applicant
HeartLung Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2022
Days to Decision
240 days
Submission Type
Summary

ABMD Software

Page Type
Cleared 510(K)
510(k) Number
K213760
510(k) Type
Traditional
Applicant
HeartLung Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2022
Days to Decision
240 days
Submission Type
Summary