Last synced on 25 January 2026 at 3:41 am

Pseudo-Patient

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180697
510(k) Type
Traditional
Applicant
Rtsafe, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2018
Days to Decision
116 days
Submission Type
Summary

Pseudo-Patient

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180697
510(k) Type
Traditional
Applicant
Rtsafe, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2018
Days to Decision
116 days
Submission Type
Summary