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Faxitron Bioptics Speciemen Radiography System

Page Type
Cleared 510(K)
510(k) Number
K170786
510(k) Type
Traditional
Applicant
Faxitron Bioptics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2017
Days to Decision
124 days
Submission Type
Summary

Faxitron Bioptics Speciemen Radiography System

Page Type
Cleared 510(K)
510(k) Number
K170786
510(k) Type
Traditional
Applicant
Faxitron Bioptics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2017
Days to Decision
124 days
Submission Type
Summary