FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Vial2Bag Advanced® 20mm Admixture Device

K Number: K240940 · Decision May 3, 2024
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
6
Review Days
28

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Basic Information

Device Name
Vial2Bag Advanced® 20mm Admixture Device
K Number
K240940
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
West Pharmaceutical Services, Inc.
Date Received
April 5, 2024
Decision Date
May 3, 2024
Product Code
LHI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LHI Set, I.V. Fluid Transfer

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K Number Device Name
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K123588 INTRADERMAL ADAPTER
K082908 NOVAGUARD, MODEL 3611001
K041691 CLIP 'N'JECT RECONSTITUTION SYSTEM (CLIP 'N'JECT