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ORIGEN REINFORCED DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K113869
510(k) Type
Traditional
Applicant
Origen Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2012
Days to Decision
209 days
Submission Type
Summary

ORIGEN REINFORCED DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K113869
510(k) Type
Traditional
Applicant
Origen Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2012
Days to Decision
209 days
Submission Type
Summary