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Concentriq Dx

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230839
510(k) Type
Traditional
Applicant
Proscia, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2024
Days to Decision
318 days
Submission Type
Summary

Concentriq Dx

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230839
510(k) Type
Traditional
Applicant
Proscia, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2024
Days to Decision
318 days
Submission Type
Summary