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

FLC Kappa, FLC Lambda, FLC Control Level 1, FLC Control Level 2

K Number: K210623 · Decision Nov 18, 2022
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
62
Applicant Total
32
Review Days
626

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Basic Information

Device Name
FLC Kappa, FLC Lambda, FLC Control Level 1, FLC Control Level 2
K Number
K210623
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5550
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sebia
Date Received
March 2, 2021
Decision Date
November 18, 2022
Product Code
DFH
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DFH Kappa, Antigen, Antiserum, Control

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K180762 CAPI 3 HEMOGLOBIN(E)
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K172195 HYDRASHIFT 2/4 daratumumab, daratumumab Control
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K162281 CAPI 3 Hb A1c, MULTI-SYSTEM Hb A1C CAPILLARY CONTROLS (2)
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