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TEGRESS IMPLANT NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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