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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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