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FDA PRODUCT CODE · CLASS II

SENBiofeedback For Adjunctive Treatment Of Symptoms Associated With Stress And Anxiety

A biofeedback device for adjunctive treatment of patient-reported symptoms associated with stress and anxiety is intended to provide feedback to users with patient-reported symptoms associated with stress and anxiety on a physiological measurement as a relaxation treatment for the reduction of stress and anxiety.

DEVICE CLASS
Class II
REGULATION
21 CFR 882.5050
MEDICAL SPECIALTY
Neurology
REVIEW PANEL
NE
ImplantLife-sustainingGMP-exemptThird-party review eligible
1
510(K)/PMA CLEARANCES
510k: 1
0
RECALL ENTRIES

Recent clearances

K233337Freespira, Inc. · 510k2025-04-24

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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