FDA 510(k) Applications for Medical Device Product Code "FDC"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K021166 | ACMI-CIRCON CORPORATION | ACMI BIPOLAR RECTOSCOPE, MODEL EIWE-BR | 05/09/2002 |
K991426 | MAHE INTL., INC. | MAHE INSTRUMENTS | 08/05/1999 |
K992141 | OLYMPUS WINTER & IBE GMBH | OLYMPUS WORKING ELEMENT FOR PROBES | 09/29/1999 |