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MODIFIED TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K020985
510(k) Type
Traditional
Applicant
TFX MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2002
Days to Decision
90 days
Submission Type
Summary

MODIFIED TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K020985
510(k) Type
Traditional
Applicant
TFX MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2002
Days to Decision
90 days
Submission Type
Summary