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AnemoCheck

Page Type
Cleared 510(K)
510(k) Number
K163215
510(k) Type
Traditional
Applicant
Sanguina, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2017
Days to Decision
301 days
Submission Type
Summary

AnemoCheck

Page Type
Cleared 510(K)
510(k) Number
K163215
510(k) Type
Traditional
Applicant
Sanguina, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2017
Days to Decision
301 days
Submission Type
Summary