EKOS MICRO-INFUSION SYSTEM— 510(k) K063620
UnknownEkos Corp.
FDA 510(k) clearance K063620 for EKOS MICRO-INFUSION SYSTEM, Unknown on 2007-08-06. Applicant: Ekos Corp.. Device class: 2.
Clearance details
- Applicant
- Ekos Corp.
- Product code
- Code QEY
- Device class
- Class 2
- Regulation
- 21 CFR 870.5150
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Bothell, WA, US
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More clearances from Ekos Corp.
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