FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Lp(a) Ultra

K Number: K211058 · Decision Dec 22, 2022
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
12
Review Days
622

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Basic Information

Device Name
Lp(a) Ultra
K Number
K211058
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5600
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SENTINEL CH. SpA
Date Received
April 9, 2021
Decision Date
December 22, 2022
Product Code
DFC
Advisory Committee
Immunology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
DFC Lipoprotein, Low-Density, Antigen, Antiserum, Control

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Other Clearances by SENTINEL CH. SpA

K Number Device Name
K242585 Cystatin C
K193001 Albumin BCP
K192118 CRP Vario
K173833 CRP Vario
K141728 ACE CALIBRATOR
K102706 CKMB UDR ASSAY
K083602 KAPPA LIGHT CHAINS
K083601 LAMBDA LIGHT CHAINS
K081533 SENTINEL PLASMAPROTEINS CAL 3X
K073634 MULTIGENT CREATININE (ENZYMATIC) ASSAY
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