Last synced on 14 November 2025 at 11:06 pm

EKOS PERIPHERAL INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K050563
510(k) Type
Special
Applicant
EKOS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2005
Days to Decision
25 days
Submission Type
Summary

EKOS PERIPHERAL INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K050563
510(k) Type
Special
Applicant
EKOS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2005
Days to Decision
25 days
Submission Type
Summary