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PLEURX PERITONEAL CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113854
510(k) Type
Traditional
Applicant
CAREFUSION
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/19/2012
Days to Decision
81 days
Submission Type
Summary

PLEURX PERITONEAL CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113854
510(k) Type
Traditional
Applicant
CAREFUSION
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/19/2012
Days to Decision
81 days
Submission Type
Summary