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Selux AST System; Model AST Gen 1.0

Page Type
Cleared 510(K)
510(k) Number
K211748
510(k) Type
Traditional
Applicant
Selux Diagnostics, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2023
Days to Decision
681 days
Submission Type
Summary

Selux AST System; Model AST Gen 1.0

Page Type
Cleared 510(K)
510(k) Number
K211748
510(k) Type
Traditional
Applicant
Selux Diagnostics, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2023
Days to Decision
681 days
Submission Type
Summary