FDA 510(k), K212525, Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices
FDA 510(k), K212525, Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices
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510(K) Number: K212525
Device Name: Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices
Manufacturer: Advcare Medical
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 08/11/2021
Decision Date: 08/19/2022
Regulation Medical Specialty: General Hospital
Device Name: Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices
Manufacturer: Advcare Medical
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 08/11/2021
Decision Date: 08/19/2022
Regulation Medical Specialty: General Hospital
- 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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