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EchoSK and EchoSGyn modules for EchoS Family devices

Page Type
Cleared 510(K)
510(k) Number
K212851
510(k) Type
Traditional
Applicant
Echolight S.p.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
3/16/2022
Days to Decision
190 days
Submission Type
Summary

EchoSK and EchoSGyn modules for EchoS Family devices

Page Type
Cleared 510(K)
510(k) Number
K212851
510(k) Type
Traditional
Applicant
Echolight S.p.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
3/16/2022
Days to Decision
190 days
Submission Type
Summary