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Ekos Corp.

FDA Regulatory Profile

Ekos Corp. appears in FDA public data with 0 recalls, 23 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 26, 2008.

Summary

Total Recalls
0
510(k) Clearances
23
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K081467EKOSONIC ENDOVASCULAR SYSTEM WITH RAPID PULSE MODULATIONJune 26, 2008
K080392EndoWave Infusion SystemApril 30, 2008
K073166ENDOWAVE INFUSION SYSTEMApril 22, 2008
K072507ENDOWAVE INFUSION SYSTEMOctober 4, 2007
K071933ENDOWAVE INFUSION SYSTEMAugust 10, 2007
K063620EKOS MICRO-INFUSION SYSTEMAugust 6, 2007
K062508NEUROWAVE MICRO-INFUSION SYSTEMDecember 5, 2006
K062507MICRO-INFUSION SYSTEMNovember 22, 2006
K060422LYSUS INFUSION SYSTEMMarch 9, 2006
K060084LYSUS INFUSION SYSTEMFebruary 7, 2006
K053437EKOS MICRO-INFUSION SYSTEMJanuary 6, 2006
K053432EKOS MICRO-INFUSION SYSTEMDecember 30, 2005
K052071LYSUS INFUSION SYSTEMAugust 16, 2005
K051319LYSUS INFUSION SYSTEMJune 15, 2005
K051225EKOS MICRO-INFUSION SYSTEMJune 10, 2005
K041826EKOS ULTRASOUND INFUSION SYSTEMApril 27, 2005
K050563EKOS PERIPHERAL INFUSION SYSTEMMarch 29, 2005
K050472LYSUS INFUSION SYSTEMMarch 11, 2005
K043269Lysus Infusion SystemDecember 22, 2004
K042456Lysus Infusion SystemSeptember 23, 2004

FDA data resources