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CONTRAST SENSITIVITY EQUIPMENT

Page Type
Cleared 510(K)
510(k) Number
K830770
510(k) Type
Traditional
Applicant
CADWELL LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1983
Days to Decision
48 days

CONTRAST SENSITIVITY EQUIPMENT

Page Type
Cleared 510(K)
510(k) Number
K830770
510(k) Type
Traditional
Applicant
CADWELL LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1983
Days to Decision
48 days