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ATHEROEDGE

Page Type
Cleared 510(K)
510(k) Number
K122022
510(k) Type
Traditional
Applicant
ATHEROPOINT LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2012
Days to Decision
78 days
Submission Type
Summary

ATHEROEDGE

Page Type
Cleared 510(K)
510(k) Number
K122022
510(k) Type
Traditional
Applicant
ATHEROPOINT LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2012
Days to Decision
78 days
Submission Type
Summary