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FDA 510(k), K850349, VIGGO ARTERIAL CANNULA
FDA 510(k), K850349, VIGGO ARTERIAL CANNULA
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$149.00 USD
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510(K) Number: K850349
Device Name: VIGGO ARTERIAL CANNULA
Manufacturer: VIGGO PRODUCTS
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 01/28/1985
Decision Date: 04/09/1985
Regulation Medical Specialty: General Hospital
Device Name: VIGGO ARTERIAL CANNULA
Manufacturer: VIGGO PRODUCTS
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 01/28/1985
Decision Date: 04/09/1985
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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