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VERSAPORT V2 BLADELESS OPTICAL TROCAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
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510(k) Number
K130435
510(k) Type
Special
Applicant
COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2013
Days to Decision
21 days
Submission Type
Summary