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Bridge Plus Occlusion Balloon (590-002)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251358
510(k) Type
Traditional
Applicant
Philips Image Guided Therapy Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2025
Days to Decision
55 days
Submission Type
Summary

Bridge Plus Occlusion Balloon (590-002)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251358
510(k) Type
Traditional
Applicant
Philips Image Guided Therapy Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2025
Days to Decision
55 days
Submission Type
Summary