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Scope Antifogging System

Page Type
Cleared 510(K)
510(k) Number
K182080
510(k) Type
Traditional
Applicant
Xodus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2018
Days to Decision
48 days
Submission Type
Summary

Scope Antifogging System

Page Type
Cleared 510(K)
510(k) Number
K182080
510(k) Type
Traditional
Applicant
Xodus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2018
Days to Decision
48 days
Submission Type
Summary