510(k) K251993

Device
Panther Fusion GI Expanded Bacterial Assay
Applicant
Hologic, Inc.
510(k) number
K251993
Product code
PCH
Decision
Substantially Equivalent (SESE)
Decision date
2025-09-25
Date received
2025-06-27
Regulation
866.3990
Classification name
Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Patricia Villarreal
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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