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AED Sinuscope

Page Type
Cleared 510(K)
510(k) Number
K170285
510(k) Type
Traditional
Applicant
National Advanced Endoscopy Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2017
Days to Decision
183 days
Submission Type
Summary

AED Sinuscope

Page Type
Cleared 510(K)
510(k) Number
K170285
510(k) Type
Traditional
Applicant
National Advanced Endoscopy Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2017
Days to Decision
183 days
Submission Type
Summary