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Neuspera Nuity System

Page Type
Cleared 510(K)
510(k) Number
K221303
510(k) Type
Traditional
Applicant
Neuspera Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2023
Days to Decision
341 days
Submission Type
Summary

Neuspera Nuity System

Page Type
Cleared 510(K)
510(k) Number
K221303
510(k) Type
Traditional
Applicant
Neuspera Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2023
Days to Decision
341 days
Submission Type
Summary