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VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882634
510(k) Type
Traditional
Applicant
VISTECH CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1988
Days to Decision
18 days

VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882634
510(k) Type
Traditional
Applicant
VISTECH CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1988
Days to Decision
18 days