Last synced on 30 May 2025 at 11:05 pm

SPECTACLE FRAMES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933991
510(k) Type
Traditional
Applicant
U.S. OPTICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1993
Days to Decision
62 days
Submission Type
Statement

SPECTACLE FRAMES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933991
510(k) Type
Traditional
Applicant
U.S. OPTICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1993
Days to Decision
62 days
Submission Type
Statement