510(k) K231017

Device
Panther Fusion AdV/hMPV/RV Assay
Applicant
Hologic, Inc.
510(k) number
K231017
Product code
OCC
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-05
Date received
2023-04-10
Regulation
866.3980
Classification name
Respiratory Virus Panel Nucleic Acid Assay System
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Jon Kukowski
Address
10210 Genetic Center Dr. San Diego CA US 92121 92121

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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