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NIAGARA TEMPORARY DUAL LUMEN CATHETERS; FLEXXICON II TEMPORARY DUAL LUMEN CATHETERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030268
510(k) Type
Abbreviated
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2003
Days to Decision
184 days
Submission Type
Summary

NIAGARA TEMPORARY DUAL LUMEN CATHETERS; FLEXXICON II TEMPORARY DUAL LUMEN CATHETERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030268
510(k) Type
Abbreviated
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2003
Days to Decision
184 days
Submission Type
Summary