FDA 510(k) Applications for Medical Device Product Code "GDF"
|
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 |