MOBILE I.V. SYSTEMS 10,20,60
FDA 510(k) clearance K080695 · decided 2008-07-01
Clearance details
- K-number
- K080695
- Device name
- MOBILE I.V. SYSTEMS 10,20,60
- Applicant
- Northwind Technologies, Corp.
- Decision
- Substantially Equivalent
- Date received
- 2008-03-11
- Decision date
- 2008-07-01
- Days to decision
- 112 days
- Clearance type
- Abbreviated
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Manchester, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.