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MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE

Page Type
Cleared 510(K)
510(k) Number
K000728
510(k) Type
Traditional
Applicant
MEDTRONIC XOMED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
15 days
Submission Type
Summary

MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE

Page Type
Cleared 510(K)
510(k) Number
K000728
510(k) Type
Traditional
Applicant
MEDTRONIC XOMED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
15 days
Submission Type
Summary