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ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA

Page Type
Cleared 510(K)
510(k) Number
K990573
510(k) Type
Traditional
Applicant
ESTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1999
Days to Decision
16 days
Submission Type
Summary

ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA

Page Type
Cleared 510(K)
510(k) Number
K990573
510(k) Type
Traditional
Applicant
ESTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1999
Days to Decision
16 days
Submission Type
Summary