Last synced on 24 May 2024 at 11:04 pm

ProstatID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212783
510(k) Type
Traditional
Applicant
ScanMed, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2022
Days to Decision
310 days
Submission Type
Summary

ProstatID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212783
510(k) Type
Traditional
Applicant
ScanMed, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2022
Days to Decision
310 days
Submission Type
Summary