Last synced on 30 September 2022 at 11:05 pm

PLEURX PLEURAL CATHETER SYSTEM, PLEURX CATHETER ACCESS KIT, PLEURX CATHETER INSERTION STYLET, PLEURX INTEGRAL VALVED PEE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121849
510(k) Type
Traditional
Applicant
CAREFUSION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2012
Days to Decision
115 days
Submission Type
Summary

PLEURX PLEURAL CATHETER SYSTEM, PLEURX CATHETER ACCESS KIT, PLEURX CATHETER INSERTION STYLET, PLEURX INTEGRAL VALVED PEE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121849
510(k) Type
Traditional
Applicant
CAREFUSION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2012
Days to Decision
115 days
Submission Type
Summary