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TEGRESS IMPLANT NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K050688
510(k) Type
Special
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2005
Days to Decision
20 days
Submission Type
Summary

TEGRESS IMPLANT NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K050688
510(k) Type
Special
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2005
Days to Decision
20 days
Submission Type
Summary