Last synced on 14 November 2025 at 11:06 pm

Neurophet AQUA

Page Type
Cleared 510(K)
510(k) Number
K220437
510(k) Type
Traditional
Applicant
Neurophet., Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/10/2023
Days to Decision
448 days
Submission Type
Summary

Neurophet AQUA

Page Type
Cleared 510(K)
510(k) Number
K220437
510(k) Type
Traditional
Applicant
Neurophet., Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/10/2023
Days to Decision
448 days
Submission Type
Summary