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KENDALL DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963446
510(k) Type
Traditional
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1997
Days to Decision
196 days
Submission Type
Summary

KENDALL DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963446
510(k) Type
Traditional
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1997
Days to Decision
196 days
Submission Type
Summary