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Parker Quality & Compliance

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510(k) clearance

Elecsys EBV VCA IgG

FDA 510(k) source

510(k) number
K260232
Applicant
Roche Diagnostics
Decision date
Oct 2, 2026
Date received
Jan 26, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
LSE
Device type
Epstein-Barr Virus, Other
Device class
Class I
Regulation
21 CFR 866.3235
Advisory committee
Microbiology
Statement or summary
Summary
Third party
N
Location
Indianapolis, IN, US