Last synced on 20 June 2025 at 11:06 pm

K-ASSAY CRP (Ver.2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242170
510(k) Type
Traditional
Applicant
Kamiya Biomedical Company, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2025
Days to Decision
268 days
Submission Type
Summary

K-ASSAY CRP (Ver.2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242170
510(k) Type
Traditional
Applicant
Kamiya Biomedical Company, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2025
Days to Decision
268 days
Submission Type
Summary