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StentBoost Mobile

Page Type
Cleared 510(K)
510(k) Number
K203623
510(k) Type
Abbreviated
Applicant
Philips India Limited
Country
India
FDA Decision
Substantially Equivalent
Decision Date
4/5/2021
Days to Decision
115 days
Submission Type
Summary

StentBoost Mobile

Page Type
Cleared 510(K)
510(k) Number
K203623
510(k) Type
Abbreviated
Applicant
Philips India Limited
Country
India
FDA Decision
Substantially Equivalent
Decision Date
4/5/2021
Days to Decision
115 days
Submission Type
Summary