FDA 510(k) Applications Submitted by JEFFREY W COBB

FDA 510(k) Number Submission Date Device Name Applicant
K020067 01/09/2002 GYRUS ENT SOMNOPLASTY GENERATOR GYRUS ENT L.L.C.
K021777 05/30/2002 GYRUS ENT COGENT 2/G2 SYSTEM (GENERATOR,ACCESSORIES SOMNOPLASTY ELECTRODES AND PLASMACISION ELECTRODES) GYRUS ENT L.L.C.
K003214 10/13/2000 SMITH & NEPHEW PISTONS GYRUS ENT L.L.C.


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