FDA 510(k) Applications for Medical Device Product Code "GDY"
(Gauze/Sponge, Internal, X-Ray Detectable)

FDA 510(k) Number Applicant Device Name Decision Date
K955599 STRYKER CORP. STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE 02/22/1996
K972634 ULTRACELL MEDICAL TECHNOLOGIES, INC. ULTRACELL SUCTION SPONGE 12/17/1997


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