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FDA 510(k) Applications for Medical Device Product Code "GEA"
(Cannula, Surgical, General & Plastic Surgery)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K003965
AESCULAP, INC.
MRI SAFE INSTRUMENTS
03/16/2001
K982472
GENICON, LC
GENICON TROCAR
02/04/1999
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