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VISITEC EYE PAD

Page Type
Cleared 510(K)
510(k) Number
K940210
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
52 days
Submission Type
Summary

VISITEC EYE PAD

Page Type
Cleared 510(K)
510(k) Number
K940210
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
52 days
Submission Type
Summary