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EKOS PERIPHERAL INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030637
510(k) Type
Traditional
Applicant
EKOS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2003
Days to Decision
144 days
Submission Type
Summary

EKOS PERIPHERAL INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030637
510(k) Type
Traditional
Applicant
EKOS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2003
Days to Decision
144 days
Submission Type
Summary