Last synced on 25 January 2026 at 3:41 am

SIMILE FLOW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052106
510(k) Type
Traditional
Applicant
Pentron Clinical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2005
Days to Decision
89 days
Submission Type
Summary

SIMILE FLOW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052106
510(k) Type
Traditional
Applicant
Pentron Clinical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2005
Days to Decision
89 days
Submission Type
Summary