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FIBER OPTIC ENDOILLUMINATION PROBE

Page Type
Cleared 510(K)
510(k) Number
K980636
510(k) Type
Traditional
Applicant
DUTCH OPHTHALMIC USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
90 days
Submission Type
Summary

FIBER OPTIC ENDOILLUMINATION PROBE

Page Type
Cleared 510(K)
510(k) Number
K980636
510(k) Type
Traditional
Applicant
DUTCH OPHTHALMIC USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
90 days
Submission Type
Summary