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

Visby Medical Respiratory Health Test

K Number: K242526 · Decision Feb 19, 2025
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
32
Applicant Total
4
Review Days
177

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Basic Information

Device Name
Visby Medical Respiratory Health Test
K Number
K242526
Device Class
FDA class 2
Clearance Type
Dual Track
Regulation Number
866.3981
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Visby Medical, Inc.
Date Received
August 26, 2024
Decision Date
February 19, 2025
Product Code
QOF
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
QOF Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QOF), ordered by most recent decision date.

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Other Clearances by Visby Medical, Inc.

K Number Device Name
K253971 Visby Medical Flu and COVID-19 Test
K251501 Visby Medical Men's Sexual Health Test
DEN240020 Visby Medical Women's Sexual Health Test