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StentBoost Mobile

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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