Last synced on 14 June 2024 at 11:05 pm

SILS PORT, MODELS SILSPT5, SILSPT12

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082619
510(k) Type
Traditional
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2008
Days to Decision
59 days
Submission Type
Summary