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RADIONICS NASHOLD BIOPSY NEEDLE - SINGLE USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032054
510(k) Type
Traditional
Applicant
RADIONICS, A DIVISION OF TYCO HEALTHCARE GROUP LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2003
Days to Decision
75 days
Submission Type
Summary

RADIONICS NASHOLD BIOPSY NEEDLE - SINGLE USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032054
510(k) Type
Traditional
Applicant
RADIONICS, A DIVISION OF TYCO HEALTHCARE GROUP LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2003
Days to Decision
75 days
Submission Type
Summary