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ECG CT Gating Device

Page Type
Cleared 510(K)
510(k) Number
K160350
510(k) Type
Traditional
Applicant
NEOCOIL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2016
Days to Decision
129 days
Submission Type
Summary

ECG CT Gating Device

Page Type
Cleared 510(K)
510(k) Number
K160350
510(k) Type
Traditional
Applicant
NEOCOIL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2016
Days to Decision
129 days
Submission Type
Summary