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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