FDA.reportPublic FDA data

510(k) K251674

Device
Fenom Flo™ FeNO Monitoring System
Applicant
Mgc Diagnostics Corporation
510(k) number
K251674
Product code
MXA
Decision
Substantially Equivalent (SESE)
Decision date
2025-11-26
Date received
2025-05-30
Regulation
862.3080
Classification name
System, Test, Breath Nitric Oxide
Medical specialty
Clinical Toxicology
Review panel
Clinical Toxicology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Arathi Sundaresan
Address
350 Oak Grove Pkwy. St. Paul MN US 55127 55127

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code MXA#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K243926Vivatmo pro-SBosch Healthcare Solutions GmbH2025-09-11
K233775Vivatmo proBosch Healthcare Solutions GmbH2024-02-22
K213611Fenom ProCaire Diagnostics, Inc.2023-06-07
K203695NObreath®Bedfont Scientific, Ltd.2021-12-17
K182874Fenom Pro Nitric Oxide TestSpirosure, Inc.2019-02-13
K170983NIOX VEROCircassia AB2017-11-22
K150233NIOX VERO Airway Inflammation MonitorAerocrine AB2015-02-26
K133898NIOX VERO AIRWAY INFLAMMATION MONITORAerocrine AB2014-11-06
K123683NIOX PANEL FOR USE WITH THE NIOX MINO AIRWAY INFLAMMATION MONITORAerocrine AB2012-12-27
K101034NIOX MINO MODEL 09-1000Aerocrine AB2010-09-02
K083617APIERON INSIGHT ENO SYSTEMApieron, Inc.2009-01-27
K073265APIERON INSIGHT EXHALED NITRIC OXIDE (ENO) SYSTEMApieron, Inc.2008-03-14
K072816NIOX MINOAerocrine AB2008-03-03
DEN030001NIOX ARTICLE NO: 02-1000Aerocrine AB2003-04-30