FDA 510(k) Applications for Medical Device Product Code "GDF"
(Guide, Needle, Surgical)

FDA 510(k) Number Applicant Device Name Decision Date
K031173 NEEDLETECH PRODUCTS, INC. NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013 07/23/2003


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