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OPTX 20/20

Page Type
Cleared 510(K)
510(k) Number
K953413
510(k) Type
Traditional
Applicant
NEOPTX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1995
Days to Decision
18 days
Submission Type
Statement

OPTX 20/20

Page Type
Cleared 510(K)
510(k) Number
K953413
510(k) Type
Traditional
Applicant
NEOPTX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1995
Days to Decision
18 days
Submission Type
Statement