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PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim Implantable Ports

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242328
510(k) Type
Special
Applicant
Bard Access Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2024
Days to Decision
86 days
Submission Type
Summary

PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim Implantable Ports

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242328
510(k) Type
Special
Applicant
Bard Access Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2024
Days to Decision
86 days
Submission Type
Summary