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

Lipoprotein (a) Molarity Assay

K Number: K253069 · Decision Jun 16, 2026
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
11
Review Days
266

Basic Information

Device Name
Lipoprotein (a) Molarity Assay
K Number
K253069
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5600
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diazyme Laboratories, Inc.
Date Received
September 23, 2025
Decision Date
June 16, 2026
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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