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SHARKCORE FINE NEEDLE BIOPSY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141894
510(k) Type
Traditional
Applicant
COVIDIEN LLC (FORMERLY BEACON ENDOSCOPIC CORP)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2014
Days to Decision
84 days
Submission Type
Summary

SHARKCORE FINE NEEDLE BIOPSY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141894
510(k) Type
Traditional
Applicant
COVIDIEN LLC (FORMERLY BEACON ENDOSCOPIC CORP)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2014
Days to Decision
84 days
Submission Type
Summary