FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

freeflex+ Transfer Adapter

K Number: K212445 · Decision Jun 1, 2022
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
12
Review Days
300

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Basic Information

Device Name
freeflex+ Transfer Adapter
K Number
K212445
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fresenius Kabi AG
Date Received
August 5, 2021
Decision Date
June 1, 2022
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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