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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Xpert Xpress CoV-2/Flu plus

FDA 510(k) source

510(k) number
K263333
Applicant
Cepheid®
Decision date
Oct 22, 2026
Date received
Sep 22, 2026
Decision
Substantially Equivalent
Clearance type
Special
Product code
QOF
Device type
Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents
Device class
Class II
Regulation
21 CFR 866.3981
Advisory committee
Microbiology
Statement or summary
Summary
Third party
N
Location
Sunnyvale, CA, US