Last synced on 18 April 2025 at 11:05 pm

PREVENT Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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