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SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133763
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2014
Days to Decision
155 days
Submission Type
Summary

SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133763
510(k) Type
Traditional
Applicant
MEDI-GLOBE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2014
Days to Decision
155 days
Submission Type
Summary