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FDA 510(k), K951739, PUMP/BLOOD CHEMISTRY MONITOR
FDA 510(k), K951739, PUMP/BLOOD CHEMISTRY MONITOR
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510(K) Number: K951739
Device Name: PUMP/BLOOD CHEMISTRY MONITOR
Manufacturer: VIA MEDICAL CORP.
Device Classification Name: pump, infusion, analytical sampling
Regulation Number: 880.5725
Classification Product Code: LZF
Date Received: 04/14/1995
Decision Date: 02/28/1996
Regulation Medical Specialty: General Hospital
Device Name: PUMP/BLOOD CHEMISTRY MONITOR
Manufacturer: VIA MEDICAL CORP.
Device Classification Name: pump, infusion, analytical sampling
Regulation Number: 880.5725
Classification Product Code: LZF
Date Received: 04/14/1995
Decision Date: 02/28/1996
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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