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ClarifEye R1.0, ClarifEye Needle

Page Type
Cleared 510(K)
510(k) Number
K201743
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederlands B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
2/23/2021
Days to Decision
243 days
Submission Type
Summary

ClarifEye R1.0, ClarifEye Needle

Page Type
Cleared 510(K)
510(k) Number
K201743
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederlands B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
2/23/2021
Days to Decision
243 days
Submission Type
Summary