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ECLERIS SINUSCOPE

Page Type
Cleared 510(K)
510(k) Number
K131323
510(k) Type
Traditional
Applicant
Ecleris USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2014
Days to Decision
397 days
Submission Type
Statement

ECLERIS SINUSCOPE

Page Type
Cleared 510(K)
510(k) Number
K131323
510(k) Type
Traditional
Applicant
Ecleris USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2014
Days to Decision
397 days
Submission Type
Statement