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FDA 510(k), K850051, VERSA-FILL 120 & FILL SET 42-50
FDA 510(k), K850051, VERSA-FILL 120 & FILL SET 42-50
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510(K) Number: K850051
Device Name: VERSA-FILL 120 & FILL SET 42-50
Manufacturer: JOHN P VITELLO
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: LHI
Classification Product Code: 01/08/1985
Date Received: 03/06/1985
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: VERSA-FILL 120 & FILL SET 42-50
Manufacturer: JOHN P VITELLO
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: LHI
Classification Product Code: 01/08/1985
Date Received: 03/06/1985
Decision Date: Substantially Equivalent (SESE)
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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