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

Flowflex Plus RSV + Flu A/B + COVID Home Test

K Number: K251749 · Decision Oct 22, 2025
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
10
Applicant Total
85
Review Days
138

Basic Information

Device Name
Flowflex Plus RSV + Flu A/B + COVID Home Test
K Number
K251749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3987
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ACON Laboratories, Inc.
Date Received
June 6, 2025
Decision Date
October 22, 2025
Product Code
SCA
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
SCA Multi-Analyte Respiratory Virus Antigen Detection Test

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