EKOS MICRO-INFUSION SYSTEM— 510(k) K063620

Unknown

Ekos Corp.

FDA 510(k) clearance K063620 for EKOS MICRO-INFUSION SYSTEM, Unknown on 2007-08-06. Applicant: Ekos Corp..

Clearance details

Applicant: Ekos Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 2006-12-05
Decision date: 2007-08-06
Decision: Unknown
Clearance type: Traditional
Location: Bothell, WA, US

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