FDA 510(k) Applications for Medical Device Product Code "FGI"
(Catheter, Urethrographic, Male)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K013360 | NEOSEED TECHNOLOGY,LLC | DFINER UROLOGICAL CATHETER | 02/20/2002 |
| K023019 | VOMED VOLZER MEDIZINTECHNIK GMBH & CO. | VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 | 12/10/2002 |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact
