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BostonSight Scleral

Page Type
Cleared 510(K)
510(k) Number
K183175
510(k) Type
Traditional
Applicant
BostonSight
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2019
Days to Decision
49 days
Submission Type
Summary

BostonSight Scleral

Page Type
Cleared 510(K)
510(k) Number
K183175
510(k) Type
Traditional
Applicant
BostonSight
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2019
Days to Decision
49 days
Submission Type
Summary