510(k) K240632

Device
Neuvotion NeuStim NN-01
Applicant
Neuvotion, Inc.
510(k) number
K240632
Product code
GZI
Decision
Substantially Equivalent (SESE)
Decision date
2024-11-22
Date received
2024-03-06
Regulation
882.5810
Classification name
Stimulator, Neuromuscular, External Functional
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Chad Bouton
Address
165 Club Rd. Stamford CT US 06905 06905

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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