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EKOS MICRO-INFUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063620
510(k) Type
Traditional
Applicant
Ekos Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
8/6/2007
Days to Decision
244 days
Submission Type
Summary

EKOS MICRO-INFUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063620
510(k) Type
Traditional
Applicant
Ekos Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
8/6/2007
Days to Decision
244 days
Submission Type
Summary