www.fdanews.com/articles/113577-covidien-gets-510-k-clearance-from-fda
Covidien Gets 510(K) Clearance From FDA
January 8, 2009
Covidien announced that the U.S. Food and Drug Administration has granted a 510(k) clearance to market the Covidien SILS Port Multiple Instrument Access Port for laparoscopic surgeries through a single incision.
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