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

Flowflex® Plus COVID-19 Home Test

K Number: K233373 · Decision Apr 19, 2024
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
13
Applicant Total
85
Review Days
200

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Basic Information

Device Name
Flowflex® Plus COVID-19 Home Test
K Number
K233373
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3984
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ACON Laboratories, Inc.
Date Received
October 2, 2023
Decision Date
April 19, 2024
Product Code
QYT
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
QYT Over-The-Counter Covid-19 Antigen Test

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Other Clearances by ACON Laboratories, Inc.

K Number Device Name
K251697 Flowflex® Plus Strep A Rapid Test Cassette; Flowflex® Plus Strep A Rapid Test Strip
K251749 Flowflex Plus RSV + Flu A/B + COVID Home Test
K250085 On Call® Sure GK Blood Glucose & Ketone Monitoring System; On Call® Sure Sync GK Blood Glucose & Ketone Monitoring System
K250377 Flowflex Plus COVID-19 + Flu A/B Home Test
K232715 Distinct® Digital Pregnancy Test
K230828 Flowflex COVID-19 Antigen Home Test
K193318 Distinct® Early Detection Pregnancy Test
K192175 On Call Express II Blood Glucose Monitoring System
K191038 On Call Express Voice Blood Glucose Monitoring System
K181527 On Call Sure Blood Glucose Monitoring System, On Call Sure Sync Blood Glucose Monitoring System
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