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VIADUCT MICROENDOSCOPE AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K011189
510(k) Type
Traditional
Applicant
ACUEITY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2001
Days to Decision
89 days
Submission Type
Summary

VIADUCT MICROENDOSCOPE AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K011189
510(k) Type
Traditional
Applicant
ACUEITY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2001
Days to Decision
89 days
Submission Type
Summary