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ACTIFRESH 400 LENS

Page Type
Cleared 510(K)
510(k) Number
K983637
510(k) Type
Traditional
Applicant
Hydron , Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/10/1999
Days to Decision
420 days
Submission Type
Summary

ACTIFRESH 400 LENS

Page Type
Cleared 510(K)
510(k) Number
K983637
510(k) Type
Traditional
Applicant
Hydron , Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/10/1999
Days to Decision
420 days
Submission Type
Summary