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FRAME-SPECTACLE

Page Type
Cleared 510(K)
510(k) Number
K933765
510(k) Type
Traditional
Applicant
CLEARVISION OPTICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1993
Days to Decision
76 days
Submission Type
Statement

FRAME-SPECTACLE

Page Type
Cleared 510(K)
510(k) Number
K933765
510(k) Type
Traditional
Applicant
CLEARVISION OPTICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1993
Days to Decision
76 days
Submission Type
Statement