Last synced on 14 November 2025 at 11:06 pm

PREVENT Kit

Page Type
Cleared 510(K)
510(k) Number
K232379
510(k) Type
Traditional
Applicant
Clear Choice Therapeutics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2024
Days to Decision
181 days
Submission Type
Summary

PREVENT Kit

Page Type
Cleared 510(K)
510(k) Number
K232379
510(k) Type
Traditional
Applicant
Clear Choice Therapeutics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2024
Days to Decision
181 days
Submission Type
Summary