Last synced on 25 January 2026 at 3:41 am

FRAME-SPECTACLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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