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KENDALL INFANT ECMO VENOVENOUS CATHETER-DUAL LUMEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895352
510(k) Type
Traditional
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1989
Days to Decision
89 days

KENDALL INFANT ECMO VENOVENOUS CATHETER-DUAL LUMEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895352
510(k) Type
Traditional
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/1989
Days to Decision
89 days