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SILS PORT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103253
510(k) Type
Traditional
Applicant
COVIDEN (FORMERLY REGISTERED AS US SURGICAL, A DIV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2011
Days to Decision
113 days
Submission Type
Summary