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SIMILE FLOW

Page Type
Cleared 510(K)
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)
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