Last synced on 14 November 2025 at 11:06 pm

NXPRO Neuromuscular Electrical Stimulation Device

Page Type
Cleared 510(K)
510(k) Number
K191181
510(k) Type
Traditional
Applicant
NeuX Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2019
Days to Decision
162 days
Submission Type
Summary

NXPRO Neuromuscular Electrical Stimulation Device

Page Type
Cleared 510(K)
510(k) Number
K191181
510(k) Type
Traditional
Applicant
NeuX Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2019
Days to Decision
162 days
Submission Type
Summary